BACKGROUND Alkylbenzenes are useful, for example, as intermediates in the production of various end products. As an embodiment of this invention, among the products which can be synthesized more efficiently using alkylbenzenes prepared in accordance with this invention are members of the family of compounds which comprise the 2-aryl propionic acid derivatives. Specifically, ibuprofen, a commercially successful, over-the-counter, analgesic can be synthesized using isobutyl benzene prepared as a raw material.

It has been known for decades that alkali metals, when reacted with alkylbenzenes, will displace benzylic hydrogens. The resulting alkylbenzene anion/alkali metal cation pair will undergo a reaction with olefins at certain temperatures to give alkylation products in which some or all saturated benzylic carbon atoms are alkylated in such a way as to replace some or all of the benzylic hydrogen atoms on a carbon atom with one aliphatic chain per benzylic hydrogen atom. Such reactions can yield a variety of products, depending on the number of saturated benzylic carbon atoms and the number of hydrogen atoms on a given benzylic carbon atom. In the commercial production of alkylbenzenes, a product of high purity is generally desired, and byproducts must be removed.

An especially serious problem with the present alkali metal catalyzed alkylation reaction is the fact that the alpha carbon of the said alkylbenzene anion can add to either carbon atom comprising the olefinic double bond, giving two alkylation products.

Moderation of reaction conditions has proven to be effective in eliminating multiple alkylations. However, inability to conveniently improve upon addition specificity has heretofore remained problematic.

The presence of isomers due to non-specific addition of the alkylbenzene to the olefinic double bond has commercial consequences. In particular, it can have a grave impact on the overall rate of production of isobutyl benzene. For example, with the current method of producing isobutyl benzene (IBB), large amounts of normal-butyl benzene (NBB)

are formed. As the boiling point of IBB (171 °C) is similar to the boiling point of NBB (183°C), distillation to high purity is greatly complicated due to the necessity of removing a byproduct with a similar boiling point. In fact, the time required to distill off enough NBB to give an IBB product of sufficient purity for the required applications can cause purification to be the rate-limiting step in the production of IBB.

In addition to isomer formation, another problem with present processes is that the alkali metal catalysts utilized in the alkylation reaction seem to exacerbate the formation of insoluble tarry byproducts. Analysis of this byproduct indicates that it is comprised of high molecular weight molecules, likely the result of an alkali metal catalyzed polymerization reaction.

Other byproducts are formed as well. These are generally soluble in the reaction mixture, and their presence may cause the reaction mixture to have a darkened color.

The formation of tars and other byproducts has serious commercial consequences, as illustrated in the large-scale production of IBB. A current commercial method for the production of IBB is carried out as a batch process using a sodium/potassium alloy. The catalyst composition is prepared in situ by charging to the reactor toluene, small amounts of tall oil and water, and an amount of NaK2 such that the mole ratio of NaK2 to toluene is about 0.024. The temperature is raised to around 190°C. After about 15 minutes, propylene is fed to a reactor pressure of about 350 psig, and a propylene to NaK2 mole ratio of about 0.028. After roughly 4-6 hours, the reaction mixture is cooled to about 50°C, and the reaction mixture is drained, and IBB is separated out. The process can be reiterated for successive batch production of IBB. Constant mechanical agitation is employed during the reaction in order to keep the catalyst and associated catalytic species emulsified; emulsification greatly increases the surface area on which benzyl potassium, the catalytically active complex in the alkylation reaction discussed above, can be formed, thus giving an enhanced reaction rate. It has been theorized that benzyl potassium coats each droplet of alloy, and that the alkylation occurs at the surface of the droplets. As the reaction proceeds, it is surmised that tar formed at the surface of a catalyst droplet accretes on the droplet, eventually encasing it. As the melting point of the tar is too high to be safely reached by the reactor, the accumulated tars inactivate large amounts of catalyst with each reaction run, making it necessary to recharge the reactor with catalyst in order to keep the reaction rate high. In addition, tar formation can shrink the reactor volume available

for formation of product, giving diminishing yields of IBB at constant energy input. Also, frequent tar plugs in reactor lines often force a complete reactor cleaning, a drastic action which results in a waste of reactants and catalyst. Tar removal is complicated by the alkali metal core of each tar granule. Known methods must be conducted with extraordinary care, as the risk of uncontrolled reaction can be high; explosions are not unknown.

The formation of isomers, tars, and other byproducts has even further commercial consequences: a negative impact on catalyst and reactant utilization. Tar encased alkali metal has a greatly reduced ability to catalyze the formation of the alkylation product desired, and it is ultimately destroyed in the tar removal process. For example, a commercial process which produces 150,000 pounds of isobutyl benzene can be expected to lose over 0.25 million dollars due to unrecycled catalyst. Furthermore, reactants which could be used to form the desired product are discarded as byproducts. In the formation of isobutyl benzene, for instance, one mole of normal-butyl benzene is formed for every nine moles of isobutyl benzene. The formation of tars and other byproducts reduces reactant utilization to about fifty percent.

Schramm and Langlois (Journal of the American chemical Society, 1960, £, 4912- 4917) present a detailed study of the effect of different alkali metals on the yield of byproducts, particularly isomers due to non-selective addition at the olefinic double bond, at a wide range of temperatures. In trials in which potassium metal was used as a catalyst in the alkylation of toluene with propylene to produce IBB, Schramm, et al. observe a roughly temperature invariant value of nine for the alkylation product ratio of isobutyl benzene (IBB) to normal butyl benzene (NBB) over the temperature range of 107°C to 204°C. In contrast, sodium catalyzes the alkylation in a temperature dependent manner, heavily favoring IBB at lower temperatures. An IBB to NBB ratio of about twelve is measured at 307°C, monotonically increasing to around twenty-four at 204°C. However, the Schramm and Langlois find that the data implies an activity for potassium that is at least an order of magnitude higher than that of sodium at all temperatures measured, specifically over the range of from 149 °C to 204°C. For example, at 149°C, sodium is expected to have an activity which is roughly one one-hundredth the activity of potassium. The activities of both metals increase monotonically with increasing temperature.

An illustration of the above findings can be seen in the current commercial process.

Despite the fact that sodium catalysis gives an IBB to NBB ratio of roughly 23 at 190°C,

Successive iterations of the process give product ratios, as defined above, of about nine, just as pure potassium gives in Schramm, et al. One might expect the sodium/potassium alloy to behave more like potassium due to sodium's relatively small activity at 190°C.

It would be of great importance if a way could be found of producing desired alkylbenzenes with greater selectivity and without formation of tars and other byproducts.

If such could be accomplished while enabling recycle of catalyst residues from run to run, the state of the art would be vastly improved.

StJMMARY OF INVENTION This invention provides novel, highly efficient process technology for the production of alkylbenzenes which makes possible the achievement of the foregoing advantages.

As the presence of tarry byproducts is a major impediment to optimum efficiency in the commercial preparation of IBB, it is desirable to reduce or eliminate their formation.

A reduction in temperature has been associated with a decline in tar production in alkali metal catalyzed alkylation reactions (Schramm, et al.), but this is accompanied by a lower IBB production rate. In light of the observation that tar formation is likely catalyzed by the alkali metal, an increase in catalyst concentration in order to counter a reduced IBB production rate may seem counterproductive. The increase in tar formation would in all likelihood decrease reactant utilization to less than the fifty percent observed in the present commercial process. In addition, the projected increase in tar formation rate would be expected to inactivate catalyst at an even greater rate.

Surprisingly, when pursuant to this invention, alkylation is carried out at a lower temperature and a mixed sodium-potassium catalyst is used at a higher concentration than used heretofore, the amount of insoluble tars is visually undetectable, and the presence of colored soluble byproducts is dramatically reduced. In addition, the reaction rate is maintained at a level comparable with the present commercial process.

Thus, in accordance with this invention, there is provided in one of its embodiments a process which comprises: A) forming a reaction mixture from components comprising (i) an alkene of greater than two carbon atoms, (ii) an alkylbenzene having at least one hydrogen atom on the alpha-carbon atom of the alkyl group, and (iii) an alkali metal alkylation catalyst composition comprising sodium atoms, potassium atoms, and an alkylbenzene, the

ratio of moles of potassium to moles of alkylbenzene being in the range of 0.01 to 0.30 moles of potassium per mole of alkylbenzene, and the atom ratio of sodium to potassium being in the range of 0.1 to 10.0 atoms of sodium per atom of potassium, and B) maintaining said reaction mixture at one or more temperatures in the range of 110°C to 180°C, at which the alkylbenzene thereof is alkylated on said alpha carbon atom to produce a reaction mass comprising (i) a longer chain alkylbenzene, and (ii) catalyst residue comprising sodium and potassium atoms, and removing at least a portion of said longer chain alkylbenzene from said reaction mass.

In conducting the process of this invention, it is possible to employ (i) fresh (i. e. virgin alkali metal alkylation catalyst composition), or (ii) a residual alkali metal alkylation catalyst composition from a prior run, or (iii) a combination of (i) and (ii). Another highly advantageous feature of this invention is that the residual catalyst composition is readily obtained from the reaction mass of a prior run conducted pursuant to this invention simply by allowing the reaction mass to stand long enough for a heavy layer comprised of catalyst residues to settle and thereafter to decant off the supernatant liquid alkylation product. All or a portion of the heavy catalyst residue can be used as a"heel"of residual catalyst in an ensuing run. Such processing was not possible in successive runs when conducting the current commercial method because of excessive tar formation.

Another beneficial feature of this invention is realized when utilizing in the alkylation reaction an asymmetrical alkene having at least one hydrogen atom on each carbon atom of the double bond. In such cases, the formation of two different isomeric products is possible depending upon the manner in which the alkylbenzene adds to such asymmetrical alkene. For example, reaction of 1-pentene with toluene tends to yield mixtures of 2-methylpentylbenzene and n-hexylbenzene. The former product involves addition to the more internal doubly-bonded carbon atom of the alkene, whereas the latter product involves addition to the less internal doubly-bonded carbon atom of the alkene.

Surprisingly, when conducting a series of runs pursuant to this invention, especially when these runs are conducted in the same reactor, the ratio of the two isomeric products tends to progressively favor formation of the product involving addition to the more internal doubly-bonded carbon atom. It has been found, for example, that in a series of alkylations pursuant to this invention involving toluene and propylene, the ratios of isobutylbenzene

to n-butylbenzene tends to increase as the number of alkylation runs increases, starting with a ratio of about 9: 1 and reaching as high as about 20: 1, or even higher, in later runs.

The trend of increasing product ratio in succeeding runs is not only highly beneficial, but is unforeseeable in light of the findings reported by Schramm, et al. to the effect that the product ratios and metal activities are affected in opposite ways by a drop in temperature. In particular, from Schramm, et al. sodium expected to exhibit an almost negligible activity at around 150°C. Thus, the conventional product ratio of 9: 1 associated with potassium could be expected for every reaction in a series. However, the present invention makes possible product ratios which reach as high as 20: 1, or more.

The above and other embodiments and features of this invention will be apparent from the ensuing description and appended claims.

Formation of Alkali Metal AlkylationCatalystCompositions The alkylbenzenes used in forming the catalyst include, for example, toluene, o- xylene, m-xylene, p-xylene, l-ethyl-2-methylbenzene, l-ethyl-3-methylbenzene, 1,3- <BR> <BR> <BR> diethylbenzene, 1, 2-diethylbenzene, 1,2, 3-trimethylbenzene, 1,2, 4-trimethylbenzene, 1,4- diethyl-3-methylbenzene, 3-isopropyl-l-methylbenzene, 4-isopropyl-l-methylbenzene, 4- isopropyl-1, 2-dimethylbenzene, 1, 2-diethyl-4-isopropylbenzene, 2, 4-diisopropyl-1- methylbenzene, 1,3, 5-triisopropylbenzene, 3-isopropyl-1-methyl-5-tert-butylbenzene, 1,3- diisopropyl-5-tert-butylbenzene, 1,3-diisopropyl-5-tert-butylbenzene, 1-isopropyl-3, 5-di- tert-butylbenzene, 2-nitro-3-methyltoluene, 3-nitro-4-methyltoluene, 3-nitro-4-ethyltoluene, <BR> <BR> <BR> <BR> 1-methoxy-2, 3-diethylbenzene, 1-ethoxy-3, 4-diethylbenzene, 1-methylthio-3-isopropyl-2- <BR> <BR> <BR> <BR> <BR> methylbenæne, l-phenoxy-2-isopropyl-3-tert-butylbenæne, 1-methoxy-3-isopropyl-2- methylbenzene, 1-ethylthio-2-isopropyl-3-tert-butylbenzene, 1-nitro-3-isopropyl-2-methyl-5- tert-butylbenzene, and analogous alkylbenzenes, preferably substituted with electron donating functional groups in one or more positions in such a way as to permit or facilitate the formation of a net negative charge on a carbon atom which is alpha to the ring.

Preferred is an alkyl-substituted toluene. Most preferred is toluene.

The original or fresh catalyst compositions can be formed (i. e., produced) from (a) sodium metal and/or organosodium compound, and (b) potassium metal and/or organopotassium compound as raw materials, in a ratio of about 0.10 to about 10.00 atoms of sodium per atom of potassium. If an organosodium and/or organopotassium compound

is used as a raw material in forming the alkali metal alkylation catalyst composition, such organosodium and/or organopotassium compound can be preformed or it can be produced in situ from the alkali metal and an appropriate reactant such as an alkene, an alkylbenzene having at least one hydrogen atom alpha to the ring, a nitroalkene having at least one hydrogen atom on the carbon atom which is alpha to a double bond, a nitroalkane having at least one acidic hydrogen atom, an alkoxyalkane having at least one acidic hydrogen atom, an alkylthioalkane having at least one acidic hydrogen atom, a nitroalkylbenzene having at least one hydrogen atom alpha to the ring, an alkoxyalkylbenzene having at least one hydrogen atom alpha to the ring, and any analogous functionally-substituted hydrocarbon having an acidic hydrogen atom.

When both metals are used in forming the initial or fresh catalytic ion pair, they can be used as individual free metals or as a mixture or alloy of sodium and potassium. An alloy with a ratio of sodium to potassium which falls in the range of 0.1 to 10.0 atoms of sodium per atom of potassium is preferred. The alloy with a ratio of sodium to potassium of about 0.5 atom of sodium per atom of potassium (NaK2) is most preferred.

When the catalytic ion pair is produced in whole or in part from organosodium compound (s) and/or organopotassium compound (s), various organocompounds of these metals can be used. For example they can be alkyl, alkenyl, cycloalkyl, cycloalkenyl, aryl, or aralkyl sodium or potassium compounds such as pentyl sodium, hexenyl sodium, phenyl sodium, naphthyl sodium, benzyl sodium, butyl potassium, propenyl potassium, phenyl potassium, cyclohexenyl potassium, 4-methylbenzyl potassium, and analogous compounds.

Of the organosodium and organopotassium compounds used in forming the fresh catalyst, it is preferred to utilize a organosodium or organopotassium compound which facilitates or permits formation of a negative charge on the carbon atom with which the sodium or potassium is associated.

To form the initial or fresh alkali metal alkylation catalyst composition, a mixture <BR> <BR> is formed from (a) sodium metal and/or organosodium compound (s), (b) potassium metal and/or organopotassium compound (s), and (c) an alkylbenzene having at least one hydrogen atom on the alpha carbon atom of the alkyl group. The proportions of these components are such that (1) the atom ratio of sodium to potassium is from about 0.1 to about 10.00, and preferably from about 0.3 to about 0.7 atom of sodium per atom of potassium (irrespective of whether such atoms are in the form of free metal or as an

organometal compound, or both), and (2) the ratio of moles of potassium (again, irrespective of whether the potassium is in the form of free metal or as an organometal compound, or both), per mole of the alkylbenzene is in the range of 0.01 to 0.30 mole of potassium per mole of alkylbenzene, and preferably in the range of 0.03 to 0.10 mole of potassium per mole of alkylbenzene. Particularly preferred is a ratio in the range of 0.03 <BR> <BR> <BR> to 0.05, (e. g., 0.045) mole of potassium per mole of alkylbenzene. The resultant mixture is heated to temperatures in the range of 90°C to 240°C, and preferably in the range of 140°C to 200°C, to form the fresh alkali metal alkylation catalyst composition. When forming the catalyst composition from sodium and potassium metals and toluene, the most preferred temperature is in the range of 170°C to 190°C, e. g. , 185°C.

Small amounts of water can be used to enhance the activity of the alkali metal. The added water is surmised to react with the alkali metal to form alkali metal oxides which improve the activity of the alkali metal in forming the catalyst composition. Preferred is a mole ratio of water to alkali metal in the range of 0.00 to 0.10. Most preferred is a ratio of about 0.04 to about 0.06. Added amounts of tall oil in the catalyst formation reaction and in the alkylation reaction have been observed to aid in the emulsification of the alkali metal catalyst composition. Preferred is a weight ratio of tall oil to total potassium in the catalyst composition in the range of 0 to 100. Most preferred is a ratio of about 1 to about 5.

The amount of time sufficient for catalyst ion pair formation can be in the range of 0.0 hours to 10.0 hours. Preferred is a time in the range of from 0.2 hours to 1.0 hours.

Most preferred is a time of about 0.5 hours.

Mechanical agitation can be beneficial to the formation of the catalyst ion pair.

Preferred is a rotary stirrer.

Typically the first alkylation run of a series of alkylation runs is conducted using a fresh alkali metal alkylation catalyst. Subsequent runs, which preferably are conducted in the same reactor, can be run using a heel containing catalyst residue from a prior alkylation run conducted pursuant to this invention and from which at least a portion of the longer chain alkylbenzene has been removed. Preferably in most, if not all, alkylation runs of a series, the reaction mixture contains both a portion of fresh alkali metal alkylation catalyst and a heel containing residual catalyst residue from a prior alkylation run. In other words, it is preferred to employ fresh catalyst as needed or as desired along with a heel containing

residual catalyst from a prior run.

Alkylation I The first alkylation reaction is generally carried out following the catalyst ion pair formation reaction. The alkylation reaction can be, and preferably is, conducted in the same reactor in which the above alkali metal alkylation catalyst composition was formed, and in such case the catalyst for the alkylation reaction is already present in the reactor.

However, it is also possible to conduct the first alkylation reaction in a separate reactor into which is charged the catalyst ion pair prepared as above, and the reactants. The alkylbenzenes which are utilized in the alkylation reaction span a wide range which comprises the alkylbenzenes referred to above in connection with formation of the alkali metal alkylation catalyst composition. Preferred is an alkyl-substituted toluene. Most preferred is toluene.

The alkenes which are suitable for use in the alkylation reaction include, but are not limited to propylene, 1-butene, 2-butene, 3-methyl-l-butene, 2-methyl-l-propene, 1- pentene, 2-pentene, 1-hexene, cyclohexene, 1-octene, 1-decene, 4-tetradecene, and other analogous olefinic hydrocarbons, as well as olefins which are substituted with suitable functionality in such a way as to permit or facilitate bond formation between 1) an alkylbenzene carbon atom which is alpha to the benzene ring on which a negative charge or a part thereof is more or less localized, and 2) either of the two carbon atoms between which existed a double bond prior to alkylation. An alkene hydrocarbon of less than five carbon atoms is preferred. Most preferred is propylene.

Typically the mole ratio of alkene to the alkylbenzene reactant in the reaction mixture is in the range of 0.01 to 10.00 moles of the alkene per mole of the alkylbenzene.

Preferably, this ratio is in the range of 0.8 to 0.9 moles of alkene per mole of the alkylbenzene reactant.

With gaseous alkene reactants, the pressure maintained within the reactor in the first alkylation should be in the range of 100 psig to 800 psig. Most preferred when using propylene or a butylene is a pressure in the range of 250 psig to 350 psig. Liquid alkenes can be reacted under subatmospheric, atmospheric or superatmospheric pressures.

A desirable mole ratio of 1) potassium in the alkali metal catalyst composition to 2) the alkylbenzene initially present in the reactor in the first alkylation reaction is typically

in the range of 0.01 to 0.30 mole of potassium per mole of such alkylbenzene. Preferred is a ratio in the range of 0.03 : 1 to 0.1 : 1. Most preferred is a ratio in the range of 0.03 : 1 to 0. 05 : 1, e. g., about 0. 045: 1.

Successful suppression of byproducts may occur at a range of temperatures.

Preferred is a temperature in the range of from 100°C to 180°C. Most preferred is a temperature in the range of from 130°C to 160°C.

The time during which the alkylation reaction mixture is maintained at reaction temperatures can be in the range of from 1 hour to 10 hours. Most preferred is a reaction period in the range of from 4 hours to 6 hours.

Separation of the desired product generally begins by allowing the residual catalytic material to settle in the reactor, followed by decanting the reactor of the remaining contents.

It is preferable during such decanting to ensure that the reactor contents remain at a minimum temperature in the range of 100°C to 180°C in order to avoid the precipitation of byproducts. Most preferred is a temperature of about 120°C. Other means of separation comprising methods such as filtration or centrifugation may be used instead of/in addition to settling and decanting. Settling and decanting is preferred. The portion containing large amounts of product can then be stored or purified as desired.

Without desiring to be bound by theory, a mechanism by which the alkylation is theorized to take place is as follows. As a result of the catalyst ion pair formation reaction, the alkali metal exists in solution as a cation, having facilitated the formation of an anion at the alpha carbon atom of the alkylbenzene and/or alkene utilized in said reaction. In the alkylation step, the alkali metal cation enables the reaction by associating with the double bond of the alkene, partially delocalizing its electrons. The resulting complex is susceptible to nucleophilic attack by the said anion, giving two possible addition products which are chain-lengthened at the alpha carbon atom. The alkali metal next associates with the carbon atom which was previously involved in the double bond, but is not presently connected to the alpha carbon of the nucleophile. Subsequently, it is replaced by the acidic alpha hydrogen atom of another molecule in the reaction mixture, recreating an anion which may repeat the above process.

Alkylation II and Successive Alkylations The alkylbenzenes which may be utilized in the second alkylation reaction comprise

the alkylbenzenes which may be utilized in the preceding reactions. In most cases the alkylbenzene used will be the same as that used in the prior run. Preferred is an alkyl- substituted toluene. Most preferred is toluene.

The alkenes which may be utilized in the second reaction comprise the alkenes suitable for the first alkylation reaction. It is preferred, but not essential, to use the same alkene in successive runs. Preferred is an alkene of less than five carbons. Most preferred is propylene.

Typically, the mole ratio of the alkene reactant to the alkylbenzene reactant in the reaction mixture prior to alkylation II and successive alkylations is in the range of 0.05 to 10.00 moles of alkene per mole of the alkylbenzene. Preferably, this ratio is in the range of 0.80 to 0.90 moles of alkene per mole of the alkylbenzene reactant.

The mole ratio of potassium present in the reactor in this run to alkylbenzene which is present in the reactor in this run may be in the range of 0.01 to 0.30 mole of potassium per mole of alkylbenzene. Preferred is a ratio of about 0.03 to about 0.10 mole of potassium per mole of alkylbenzene. Most preferred is a ratio in the range of 0.03 to 0.05, e. g., 0.045.

The reaction mixture in the second and succeeding runs can be a heel containing all or a portion of the residual catalyst from a prior run, and from which at least a portion of the longer chain alkylbenzene product has been removed. Preferably, however the catalyst composition used is the combination of (1) fresh alkali metal alkylation catalyst composition prepared as described above, and (2) a heel from a prior alkylation reaction mass containing residual alkali metal-containing catalyst residues and from which reaction mass at least a portion of the longer chain alkylbenzene product has been removed.

Small amounts of water can be included in the reaction mixture of to enhance the catalytic activity of the alkali metal alkylation catalyst composition. Preferred is a mole ratio of water to potassium in the range of 0.0 to 0.1. Most preferred is a ratio in the range of 0.04 to 0.06 moles of water per mole of potassium. Small amounts of tall oil can be added as well. Preferred is a weight ratio of tall oil to potassium in the range of 0 to 100 parts of tall oil per part of potassium. Most preferred is a ratio of about 1 to about 5 parts by weight of tall oil per part by weight of potassium.

The ratio of potassium charged to the reactor to alkene charged to the reactor may be in the range of 0.0 to 0.03 moles of potassium per mole of alkene. Preferred is a ratio

of from about 0.00 to about 0.01 mole of potassium per mole of alkene. Most preferred is a ratio of about 0.007.

A desirable ratio of sodium to potassium in the reaction mixture (whether from recycled catalyst residue in a heel from a prior run, or from a combination of recycled catalyst residue in a heel from a prior run plus fresh catalyst) is within the range of 0.1 to 10.0 atoms of sodium per atom of potassium. Preferable is a ratio of about 0.3 to about 0.7 atom of sodium per atom of potassium. Most preferable is a ratio of about 0.5.

With gaseous alkene reactants, the pressure maintained within the reactor in these alkylation runs should be in the range of 100 psig to 800 psig. Most preferred when using propylene or a butylene is a pressure in the range of 250 psig to 350 psig. Liquid alkenes can be reacted under subatmospheric, atmospheric or superatmospheric pressures.

It is desirable that the temperature at which the reaction is conducted be in the range of from 100°C to 180°C. Preferred is a range of from 130°C to 160°C. Most preferred is a temperature in the range of 145°C to 155°C, e. g. , 150°C.

The time over which the reaction is conducted may be in the range of 1 hours to 10 hours. Preferred is a range of from 4 hours to 6 hours. Most preferred is a time of about 5 hours.

Separation of desired products may be accomplished as in the first alkylation run.

The alkylation process set forth above may be repeated many times in succession as desired. The mechanism discussed in the previous section is relevant in this section as well.

The practice of this invention is illustrated by the following non-limiting example.

EXAMPLE Preparaiion XIsobutvlbenz. ene Charge to an empty reactor at ambient temperature, toluene (13,140 pounds), and tall oil (2 pounds), to form a mixture containing 250 ppm of water. Charge NaK2 (320 pounds) to the reactor and heat the contents to 190°C for 0.5 hour, using mechanical agitation to maintain NaK2 as an emulsion. Cool the reactor to 150°C, and charge propylene (5130 pounds) to a pressure of 300 psig. Maintain the reactor temperature at 150°C for 90 minutes with continuous mechanical agitation. Cool the reactor to 120°C, and vent off propylene to a pressure of 20 psig. Turn off the agitator and allow the catalyst phase to settle, and decant off the remainder of the superposed reaction mass, so that the

reactor contains the residual catalyst composition. Restart the agitator, and charge to the reactor a mixture of toluene (12,120 pounds) which has been preheated to 120°C, tall oil (1 pound), and NaK2 (40 pounds), which mixture has a water content of 130 ppm. Raise the reactor temperature to 150°C, and charge propylene (4700 pounds) to a pressure of 300 psig. Agitate the reaction mixture for 90 minutes at about 150°C. Cool the reactor to 120°C, and vent off propylene to a pressure of 20 psig. Turn off the agitation, allow the catalyst phase to settle, and decant off the remainder of the reaction mass which disposed above the settled catalyst. The alkylation is then repeated successively 12 more times using the combination of fresh catalyst (NaK2) and a heel of the catalyst residue from the immediately preceding run. The amounts of materials charged to the reactor in each run and the results achieved in each such run are summarized in the following table.

TABLE | 68tn) Lb Lhs ç9p) EDt |} =NÇplsbs BB | PBB | I} B2sr3 1 250 2 13140 5130 320 7961 56. 1 1 6. 2 9. 0 12502131405130320796156. 16. 29. 0 2130112120470040872355. 96. 29. 0 3130112040470040894257. 35. 99. 7 4130112040470040911358. 45. 211. 3 5170112040470040895757. 44. 911. 7 6170112040473040937260. 14. 712. 8 7170112040420040917554. 54. 512. 1 8270112040470040960157. 84. 911. 8 9270112040470040966458. 24. 812. 1 10270112040470040965158. 14. 712. 5 11112040470040969758. 44. 513. 1 12-112040470040950557. 24. 612. 5 13 - l 12040 4700 80 9465 57. 0 4. 6 12. 4 14-112040470050946557. 04. 413. 0 It is to be understood that the reactants and components referred to by chemical name or formula anywhere in the specification or claims hereof, whether referred to in the singular or plural, are identified as they exist prior to coming into contact with another

substance referred to by chemical name or chemical type (e. g., another reactant, and a solvent). It matters not what preliminary chemical changes, transformations and/or reactions, if any, take place in the resulting mixture or solution or reaction medium as such changes, transformations and/or reactions are the natural result of bringing the specified reactants and/or components together under the conditions called for pursuant to this disclosure. Thus the reactants and components are identified as ingredients to be brought together in connection with performing a desired chemical reaction or in forming a mixture to be used in conducting a desired reaction. Accordingly, even though the claims hereinafter may refer to substances, components and/or ingredients in the present tense ("comprises","is, etc.), the reference is to the substance, component or ingredient as it existed at the time just before it was first contacted, blended or mixed with one or more other substances, components and/or ingredients in accordance with the present disclosure.

Without limiting the generality of the foregoing, as an illustrative example, where a claim specifies that a catalyst is a palladium compound in combination with a tertiary phosphine ligand, this phraseology refers to the makeup of the individual substances before they are combined and/or mixed separately or concurrently with one or more other materials, and in addition, at the time the catalyst is actually performing its catalytic function it need not have its original makeup -- instead whatever transformations, if any, that occur in situ as the catalytic reaction is conducted is what the claim is intended to cover. Thus the fact that a substance, component or ingredient may have lost its original identity through a chemical reaction or transformation during the course of contacting, blending or mixing operations, if conducted in accordance with this disclosure and with the application of common sense and the ordinary skill of a chemist, is thus wholly immaterial for an accurate understanding and appreciation of the true meaning and substance of this disclosure and the claims thereof.