USRE23916E - Oxidation of aromatic hydrocarbons - Google Patents

Oxidation of aromatic hydrocarbons Download PDF

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USRE23916E
USRE23916E US23916DE USRE23916E US RE23916 E USRE23916 E US RE23916E US 23916D E US23916D E US 23916DE US RE23916 E USRE23916 E US RE23916E
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hydroperoxide
oxidation
oxygen
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C409/00—Peroxy compounds
    • C07C409/02—Peroxy compounds the —O—O— group being bound between a carbon atom, not further substituted by oxygen atoms, and hydrogen, i.e. hydroperoxides
    • C07C409/04—Peroxy compounds the —O—O— group being bound between a carbon atom, not further substituted by oxygen atoms, and hydrogen, i.e. hydroperoxides the carbon atom being acyclic
    • C07C409/08—Compounds containing six-membered aromatic rings
    • C07C409/12—Compounds containing six-membered aromatic rings with two alpha,alpha-dialkylmethyl hydroperoxy groups bound to carbon atoms of the same six-membered aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
    • C07C37/08—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by decomposition of hydroperoxides, e.g. cumene hydroperoxide
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C407/00—Preparation of peroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C407/00—Preparation of peroxy compounds
    • C07C407/003—Separation; Purification; Stabilisation; Use of additives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C409/00—Peroxy compounds
    • C07C409/02—Peroxy compounds the —O—O— group being bound between a carbon atom, not further substituted by oxygen atoms, and hydrogen, i.e. hydroperoxides
    • C07C409/04—Peroxy compounds the —O—O— group being bound between a carbon atom, not further substituted by oxygen atoms, and hydrogen, i.e. hydroperoxides the carbon atom being acyclic
    • C07C409/08—Compounds containing six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
    • C07C45/517—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of peroxy-compounds to >C = O groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
    • C07C45/53—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition of hydroperoxides
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S260/00—Chemistry of carbon compounds
    • Y10S260/28—Peroxide

Definitions

  • This invention relates to a process of oxidizing an alkylwere taken at periodic intervals for refractive indextand hydroperoxide determinations, the hydroperoxide content of the oxidized oil being determined by adding a thing: or the oil to acidified potassium iodide and noting amount of iodine liberated.
  • the substituted aromatic organic compound having the structural formula Bi /H )a Rs A! in which R1 and R2 represent alkyl groups and Ar represents an alkaryl group containing two or more carbon atoms in the alkyl side chain. More particularly, the invention relates to theoxidation of compounds such as diisopropylbenzene in the liquid phase by means of molecular oxygen.
  • manganese naphthenate for example, is dissolved in p-diis'opropylbenzene and the latter then is agitated vigorously while a stream of air or oxygen is simultaneously blown through the reaction mixture.
  • the reaction is carried out at a temperature between about 40 and about 70 C. until -standard analytical data such as refractive index indicate the conversion of ap roximately 30 to 70% of the p-diisopropylbenzene.
  • the reaction mixture then may be worked up to recover a reaction product containing preponderant amounts of una-dimethyI- p-isopropylbenzyl hydroperoxide.
  • the reaction product At the-higher levels of conversion tov hydroperoxide the reaction product also will contain a considerable amount of u.a,a.'-tetramethyl-pxvlylene dihydroperoxide, which crystallizes easily from the reaction mixture.
  • EXAMPLE 1 been dissolved was placed in a closed reaction vessel equipped with a reflux condenser, a gas inlet tube openin through a porous fritted-glass plate, a thermometer, and
  • oxidized oils had a refractive index of 1.4972 and contained 19.6% hydroperoxide.
  • the refractive index was 1.5005 (approximately 58% conversion) and the amount of a-dimethyl-p-isopropylbenzyl hydroperoxide was 34.6%.
  • Example 2 The process of Example 1 was duplicated with the ex-' ception that the reaction was run for a much longer length of time and the temperature was raised to 50' C. at the end of 75 hours.
  • the refractive index of the oily reaction mixture was 1.4972, this indicating a conversion of about 40%, and the hydroperoxide content was 26.9%.
  • the hydroperoxide content was 29.3%.
  • the refractive index was 1.4986 and the hydroperoxide content was 31.8%.
  • U on completion of 49 hours of oxidation an additional 1.25 parts of manganese naphthenate was addedto the reaction mixture.
  • the hvdroperoxide content was 32.6%.
  • the refractive index was 1.5002, this indicating a conversion of about 55%, and the hydroperoxide content was 36.4%.
  • the temperature was raised to 50 C. upon completion of 75 hours of oxidation and the reaction continued at this temperature for an additional 24 hours.
  • the refractive index of the oily reaction mixture was 1.5012. this corresponding to a conversion of about and the amount of ,a-dimethyl-pisopropylbenzyl hydroperoxide was 39.2%.
  • EXAMPLE 3 One hundred thirty-eight parts of p-ethylisopropyibem, zene (refractive index at 20' C., 1.4932: boiling point at 67 mm./sq. cm. pressure. 115.4-115.8 C.) in which 0.7 part of manganese naphthenate of 6% manganese content had been dissolved was charged into a closed reaction vessel equipped with a reflux condenser, a gas inlet tube opening through a porous fritted-glass plate, a thermometer. and an efficient high-speed agitator. The reaction mixture was heated to 50 C.
  • reaction vessel was At the end of 18 hours the color of the reaction mixture turned to light amber, the refractive index was 1.4995, and
  • EXAMPLE 4 Five thousand parts of commercial d of lead naphthenate of 32% lead content had been dissolved was placed in a nickel autoclave equipped with a reflux condenser, n stirrer (200 R. P. M.) and designed for high-presure oxidations. The autoclave also was charged with207partsofoxidizedcumenetoinitiatethereaciisopropylbenzene (refractive index at'20' C., 1.4899) in which 15.6 part same tion, this oxidzed cumene containing 12.2% a',u-dimethylbe'nzyl hydroperoxide. Oxygen was passed through the the oxidation the temperature within the autoclave was maintained at 120 C.
  • the examples have set forth the use of diisopropylbenacne and p-ethylisopropylbenzene as the compoundsto which the oxidation has been applied, but other com pounds having the structural formula previously set forth for the alkyl-substituted aromatic organic com poundsmay be utilized; Exemplary of such are triiso- P Pylbenzene and p-butylisopropylbenzene.
  • the main requirement for the compounds which may be oxidized in accordance with thisinvention is the presenceof a. tertiary carbon atom carrying a hydrogen atom as its fom'th substituent.
  • the alkarvl group need not be derived'from benzene as'is the case' in diisopropylbenzene.
  • Compounds containing aromatic nuclei such as those derived from naphthalene, anthracene and phenanthrene also are operable, but some of. these compounds, being solids, must be dissolved in ,a suitable solvent. such as benzene, during the liquid phase oxidation.
  • the alkaryl group essentiallv is an aromatic nucleus substituted with one or more alkyl groups containing two or more carbon atoms. Representative alkyl groups composing pounds per square inch, the rate of input may be from per hour per kilogram of the alkaryl compound, a pre erable ran being from about $0 to about 280 liters per hour per ograrn.
  • the oxidation process of this-invention is carried out in the presence of a catalytically active heavy metal compound, particularly of such metals as manganese, cobalt, lead, iron, nickel, copper, vanadium, chromium and mercury.
  • a catalytically active heavy metal compound particularly of such metals as manganese, cobalt, lead, iron, nickel, copper, vanadium, chromium and mercury.
  • the oxides, hydroxides, or organic acid salts of any of these metals or combinations thereof which are phthalate, manganese linoleate, manganese naphthenate,
  • alkyl side chain portion of the alkaryl group may be illustrated by the ethyl group in p-ethylisopropylbenzene,
  • the isopropyl group in p-diisopropylbenzene and the two isopro yl groups in triisopropvlbenzene and the groups may, for. example. be ethyl, propyl. isopropyl. butyl. isobutyl'. secondary butvl, tertiary butyl, and the like.
  • a tertiary carbon atom carrying a hydrogen atom as its fourth substituent. are capable of being oxidized to dihydroperoxides.
  • diisopropylbenzene which may be oxidized to a,a,a',
  • compounds containing two tertiary alkvl substituents in the alkaryl group may be oxidized to trihydro eroxides.
  • Exemplary of such compounds is triisopropylbenezene.
  • the alkyl substituents in the .alkaryl groups may, in other words, have the same configuration as the tertiary alkyl' in the structural formula-shown previously
  • the alkyl groups as represented bv R1 and R: in the structural formula need not be limited to the methyl groups of pethylisopropylbenzene and diisopropylbenzene.
  • Other alkyl groups such as those previously indicated as suitable in composing the alkvl substituents of the alkaryl groups may be utilized, and R1 and R: may be either the same or difierent.
  • the examples have set forth the use of molecular oxygen as the oxygen-containing gas'but air also may be used.
  • the oxygen may be furnished also in mixtures of oxygen with nitrogen or other inert gases.
  • Oxygen when used alone, may be in the form of pure or commercial oxygen. Air may be utilized either as it is readily available or as humidified up to the saturation point.
  • the rate of input of the oxygen-containing gas may vary within a wide range
  • cobalt naphthenate mixed lead-cobalt naphthenate
  • the heavy metal resinates such as manganese, lead or cobalt resinate.
  • the resinates may be derived from any rosin acid, such as abietic, piman'c, dehydroabietic, dihydroabietic or tetrahydroabietic acid.
  • 'Ihose oxidized oils obtained according to the process of this invention and containing preponderant amounts of hydroperoxides are useful in initiating the oxidation reaction by relieving inhibitions caused by harmful impurities.
  • 'Ihese oxidized oils do not act as actual catalysts and are therefore highly desirable initiators for those oxidations which exhibit inhibition.
  • the concentration of the catalytically active heavy metal compound is critical in obtaining high hydroperoxide yields. If the concentration of the catalyst is too low, the reaction is too slow and if the catalyst concentration is higher than the maximum value utilized in accordance 1 with this invention, the yield of hydroperoxide wil be adversely affected. In general, high hydroperoxide yields may be obtained if the concentration of the catalyst in solution in the oxidation reaction mixture is at any particular instant from about 0.15 to about 0.8% based on the alkyl-substituted aromatic organic compound.
  • a preferable range on this basis is from about 0.2 to about 0.6%, and a particularly applicable range is from about 0.25 to about 0.5 Since many of the heavy metals have a tendency to precipitate as peroxides, such as manganese dioxide, from, for example, their salts with organic acids, it may be necessary from time to time to add an additional amount of the catalyst inorder to maintain the desired catalyst concentration. Within the ranges of catalyst concentration, the amount of any particular catalyst will vary somewhat depending upon the metal content and activity of the catalyst. It is possible, for example, in the preparation of the heavy metal salts of organic acids to'vary the amount of metal contained in the final salt, consequently smaller amounts of a salt containing a relatively high metal content will be needed in comparison to the same salt containing a smaller amount of the metal.
  • cobalt salts are more active than the manganese and lead salts, and the naphthenates are more active than the linoleates, which in turn are more active than the acetates. Consequently, a smaller amount of cobalt naphthalene, for example, will be needed than will be needed in the case of lead naphthenate or manganese linoleate.
  • hydroperoxide-rich oils which may be used to initiate the oxidation reaction, these oils may be used in amounts varying from about I to about 50% based onthe alkyl-substituted aromatic organic gggpound, but a preferable range is from about 2 to about a
  • the temperatures at which the oxidations are carried out also are quite critical in obtaining optimum yields of hydroperoxides. The temperatures which actually may be used,- however, will depend 'on thepressure existing during the oxidations. Upon the basis of atmospheric pressure, the temperature should be in the range of about 40' to about 70' C., a more desirable range being between about and about 65' C., and avparticularly advantageous range being between about and about C. The minimum temperature of 40 C.
  • Temperatures greater than 10 C. may be used, how ever, in the process of this invention providing the pressure is increased to greater than atmospheric. Although elevation of the temperature 'during the oxidation to greater than 70 C. will cause increased decomposition of the hydroperoxides to ketones, this is offset by the in creased rate of hydroperoxide formation caused by the elevation of the pressure. Also, it is possible to hinder the decomposition of the hydroperoxides to ketones, as caused by elevation of the temperature, by using a low activity catalyst such as lead naphthenate or linoleate, and
  • the process of this invention therefore may be carried out at temperatures between about 40 and about 140 C., a more desirable range being between about 45 and about 130 C., and a particularly advantageous range between about 50' and about'120 C.
  • pressures which can be utilized during those oxidations carried out at greater than atmospheric pressure are limited only by equipment design. From a practical standpoint pressures from atmospheric up to about 500 pounds per square inch are feasible. A preferable range is from about 50 to about 200 pounds per square inch.
  • reaction is heterogeneous, suitable agitation is necessary. It is particularly important to bring the air, oxygen, or other oxygen-containing gas into intimate con tact with the liquid phase, and this may be effected by using high-speed stirrers, suitable nozzles, porous plates or their combinations.
  • the course of the reaction may be followed by taking samples at intervals and determining the refractive index of the oily material.
  • refractive index values between about 1.4955 and about 1.5030 indicate that about 30 to about 70% of the original organic material has been oxidized, and the reaction then is advisably interrupted. Conversions from about 30 to about 70% can easily be obtained in the process of this invention and it isdesirable in obtaining high hydroperoxide yields to carry the conversion up to about 50-70%, since it generally is not until this conversion value is exceeded that undue amounts of sec- 'ondary products such as the corresponding. alcohol or ketone are formed.
  • the method utilized in recovery of the reaction products will vary depending upon the use to which the hydroperoxide is to be put. If the use of the hydroperoxide does not require separation of the hydroperoxide from other components, such as alcohols, ketones and unreacted starting material which may be present in the crude reaction mixture, the oily reaction product may be filtered through a layer of some filter aid to remove the catalyst by adsorption, then washed with dilute'aqueous alkali and used either in the wet, slightly cloudy state for various purposes or after clarification and drying by filtration.
  • the dilute aqueous alkali used in the washing step may be sodium hydroxide, sodium carbonate, sodium bicarbonate, and the like, the concentration of these alkalies in aqueous solution ranging from about 1 to about 10%, .but preferably from about 2 to about 5%. If it is desired, however, to obtain a highly concentrated hydroperoxide, the crude reaction product, after the alkali wash, may
  • hydroperoxides themselves formation of secondary 6 ingtheh droperoxldesfmmthecrudeoilyreactionproduct invo ves precipitation of the hydroperoxide with a concentrated aqueous solution ,(25 to ofsodium hydroxide.
  • the precipitate is crystalline and on the basis of analysis is a compound of the hydroperoxide with sodium hydroxide and water.
  • the oxidation according to this invention apparently roceeds by a peroxide mechanism.
  • a hydroperoxide is formed on the tertiary carbon atom of one of the isopropyl groups.
  • a very small fraction of the hydroperoxide is decomposed, resulting in the formation of free radicals which are sufficient to initiate the formation of more hydroperoxide molecules. If the concentration of the catalyst exceeds the amount specified in accordance with this invention, increasing.
  • hydroperoxide will decompose, resulting in an accelerationof the over-all oxidation, but decreasing the amount of undecomposed hydroperoxide at the expense of the roducts su'chas alcohols and itetones. That the oxidation follows a chain mechanism is shown by the existence of an induction period, by cases of inhibition, and by the fact that both may be eliminated by the addition of hydroperoxide-rich oils from a previous oxidation run.
  • the process of this invention is advantageous in that it has been found possible by proper selection of catalyst concentration and temperature to obtain aryl(dialkyl)- methyl hydroperoxides. These hydroperoxides are highly useful and find various commercial applications.
  • the process of p aring a substantial yield of a tertiary hydroperoxide w ich comprises passing an oxygen-containing gas through an alkyl-substituted aromatic organic compound having the structural formula Rt H in liquid phase in the an organic isers.
  • R1 and R2 representing alkyl groups and Ar represent-- ing an alkaryl group containing two or more carbon atoms in the alkyl side chain.
  • the process of p aring a substantial yield of a tertiary h xide w ich comprises passing an oxygen-contaming gas through an alkyl-substituted aromatic organic compound having the structural formula Rs Ar in liquid phase in the presence of a heavy metal salt of an organic acid, the concentration of the heavy metal salt in solution in the oxidation. reaction mixturebeing from about 0.25 to about 0.5%, based on the alkyl-substituted aromatic compound, and in the structural formula R1 and R: representing alkyl groups and Ar representing an alkaryl group containing two or more carbon atoms in the alkyl side chain.
  • the process of preparing a substantial yield of a tertiary hydroperoxide which comprises passing an oxygen-containing gas through an alkyl-substituted aromatic compound having the structural formula in liquid phase in the presence of a manganese salt of an organic acid, the concentration. of themanganese salt in solution in the oxidation reaction mixture being from about 0.15 to about 0.8%, based on the alkylsubstituted aromatic compound, and in the structural formula R1 and R: representing alkyl groups and Ar representing an alkaryl group containing two or more carbon atoms in the alkyl side chain.
  • the process of preparing a substantial yield of a tertiary hydroperoxide which comprises passing an oxygen-containing gas through an alkyl-substituted aromatic organic compound having the structural formula in liquid phase in the presence of manganese naphthenate, the concentration of the manganese naphthenate in solution in the oxidation reaction mixture being from about 0.15 to about 0.8%, based on the alkyl-substituted aromatic compound, and in the structural formula R1 and Rz representing alkyl groups and Ar representing an alkaryl group containing two or more carbon atoms in the alkyl side chain.
  • mmpflgqg .ani diisopropyl t ne in the liquid phase in the presence of a heavy metal salt of an organic acid concentration of the heavyfmetal. salt in solution in the oxidation reaction mixture being from about 0.15 to about 0.8%,-based on the, p-diisopropylbenzene.
  • dimethyl -p-isopropylbenzyl hydroperoxide which prises, passing oxygen through pdiisopropylbenzene in the liquid phase in the presence of manganese naphthenate, the concentration of the manganese naphthenate in solution in the oxidation reaction mixture being from.
  • the process 6 preparing a substantial butylisopropylben'zene hydroperoxide which comprises 7.
  • the process of preparing a s ubstantial yield of a tertiary hydroperoxide which comprises passing oxygen through an alkyl-substituted aromatic organic compound having the structural formula passing an oxygencontaining gas through p-butylisopropylbenzene in the liquid phase in the presence of a heavy metal salt of an organic acid, the concentration of the heavy metal salt in solution in the oxidation reaction mixture being from about 0.15 to about 0.8% based on the 1ributylisopropylbenzene.
  • e process of preparing a substantial yield of triisopropylbenzene trihydroperoxide which comprises passing an oxygen containing gas through triisopropylbenzene in the liquid phase in the presence of a heavy metal salt of an organic acid, the concentration of the heavy metal salt in the solution in the oxidation reaction mixture being from about 0.15 to about 0.8% based on the triisopropylbenzene.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Polymerization Catalysts (AREA)
  • Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)

Description

United States Patent Oflice Re. 23,916 Reissues]. Dec. 28, 1954 23,916 I oxrmmon on AROMA'IIC'HYDROCARBONS Eugene LM Del andJolmEReeoe, shsimonslslanlhGa alignorstoflercnlcsPowder Company, Del, a corporation of Dellware No Drawing. Original No. 2,664,447 dated December 29, 1953, Serial No. 31,394, June 5, i948. Application for reissue February 16, 1954, Serial No. 410,748
15 Claims. (Cl. 260-610) Matter enclosed in heavy brackets [1] appears in the originalpatentbutforlnsnopartotthbreissuespeclflcation; matter printed in Italics indicates the additions made by reissue.
This invention relates to a process of oxidizing an alkylwere taken at periodic intervals for refractive indextand hydroperoxide determinations, the hydroperoxide content of the oxidized oil being determined by adding a thing: or the oil to acidified potassium iodide and noting amount of iodine liberated. At the end of 19 hours the substituted aromatic organic compound having the structural formula Bi /H )a Rs A! in which R1 and R2 represent alkyl groups and Ar represents an alkaryl group containing two or more carbon atoms in the alkyl side chain. More particularly, the invention relates to theoxidation of compounds such as diisopropylbenzene in the liquid phase by means of molecular oxygen.
Prior to the process of this invention the oxidation of compounds such as diisopropylbenzene was foundto lead to the formation of products containing considerable amounts of ketones and alcohols. In the oxidation of p-diisopropylbenzene, for example, the oxidation led primarily to the formation of p-isopropyl acetophenone and a,-dimethyl-p-isopropylbenzyl alcohol. successful process for efiecting the preparationof sub- There was no stantial yields of a,u-dimethyl-p-isopropylbenzyl hydroperoxide or of a,a,s',a'-tetramethyl-p xylylene dihydroperoxide from p-diisopropylbenzene.
Now in accordance with this invention it has been found that the preparation of tertiary hydroperoxides from alkylsubstituted aromatic organic compounds having the above structural formula may be carried out by passing an oxygen-containing gas through said compounds in the liquid phase at moderately elevated temperatures in the presence of low concentrations of a catalytically active heavy metal compound. 1
in carrying out the process of this invention manganese naphthenate, for example, is dissolved in p-diis'opropylbenzene and the latter then is agitated vigorously while a stream of air or oxygen is simultaneously blown through the reaction mixture. The reaction is carried out at a temperature between about 40 and about 70 C. until -standard analytical data such as refractive index indicate the conversion of ap roximately 30 to 70% of the p-diisopropylbenzene. Utilizing known techniques the reaction mixture then may be worked up to recover a reaction product containing preponderant amounts of una-dimethyI- p-isopropylbenzyl hydroperoxide. At the-higher levels of conversion tov hydroperoxide the reaction product also will contain a considerable amount of u.a,a.'-tetramethyl-pxvlylene dihydroperoxide, which crystallizes easily from the reaction mixture.
The following examples constitute specific illustrations of the process of this invention. All amounts are based on parts by weight. I
EXAMPLE 1 been dissolved was placed in a closed reaction vessel equipped with a reflux condenser, a gas inlet tube openin through a porous fritted-glass plate, a thermometer, and
oxidized oils had a refractive index of 1.4972 and contained 19.6% hydroperoxide. The refractivs index indicated a conversion of approximately 40% of the diisopropylbenzene to oxidized materials. At the end of 43 hours the refractive index was 1.5005 (approximately 58% conversion) and the amount of a-dimethyl-p-isopropylbenzyl hydroperoxide was 34.6%.
EXAMPLE 2 The process of Example 1 was duplicated with the ex-' ception that the reaction was run for a much longer length of time and the temperature was raised to 50' C. at the end of 75 hours. At the end of 24 hours the refractive index of the oily reaction mixture was 1.4972, this indicating a conversion of about 40%, and the hydroperoxide content was 26.9%. At the end of 31 hours the hydroperoxide content was 29.3%. At the end of 48 hours the refractive index was 1.4986 and the hydroperoxide content was 31.8%. U on completion of 49 hours of oxidation an additional 1.25 parts of manganese naphthenate was addedto the reaction mixture. At the end of hours the hvdroperoxide content was 32.6%. Upon completion of 74 hours of oxidation the refractive index was 1.5002, this indicating a conversion of about 55%, and the hydroperoxide content was 36.4%. The temperature was raised to 50 C. upon completion of 75 hours of oxidation and the reaction continued at this temperature for an additional 24 hours. At this time the refractive index of the oily reaction mixture was 1.5012. this corresponding to a conversion of about and the amount of ,a-dimethyl-pisopropylbenzyl hydroperoxide was 39.2%.
EXAMPLE 3 One hundred thirty-eight parts of p-ethylisopropyibem, zene (refractive index at 20' C., 1.4932: boiling point at 67 mm./sq. cm. pressure. 115.4-115.8 C.) in which 0.7 part of manganese naphthenate of 6% manganese content had been dissolved was charged into a closed reaction vessel equipped with a reflux condenser, a gas inlet tube opening through a porous fritted-glass plate, a thermometer. and an efficient high-speed agitator. The reaction mixture was heated to 50 C. Through the inlet tube oxygen was introduced at a rate of 10 liters per hour per kilogram of p-ethylisopropylbenzene. The reaction was intiated by the addition of 7.16 parts of oxidialed cumene, this oxidized cumene containing 58.2% a,n i=dimethylbenzyl hydroperoxide. The color of the reaction mixture turned deep brown and an exothermic reaction took place. Heating was stopped and the reaction mixture cooled to remove the excess reaction heat.
an eflieient highspeed agitator. The reaction vessel was At the end of 18 hours the color of the reaction mixture turned to light amber, the refractive index was 1.4995, and
the hydroperoxide content 10.2%. An additional amount oxide.
EXAMPLE 4 Five thousand parts of commercial d of lead naphthenate of 32% lead content had been dissolved was placed in a nickel autoclave equipped with a reflux condenser, n stirrer (200 R. P. M.) and designed for high-presure oxidations. The autoclave also was charged with207partsofoxidizedcumenetoinitiatethereaciisopropylbenzene (refractive index at'20' C., 1.4899) in which 15.6 part same tion, this oxidzed cumene containing 12.2% a',u-dimethylbe'nzyl hydroperoxide. Oxygen was passed through the the oxidation the temperature within the autoclave was maintained at 120 C. and the pressure of 60 pounds superatmospherlc pressures, for example, 50 to 200 v about50 to about 350 liters per square inch. Upon completion of the oxidation there was obtained. 5440 parts of cmde reaction product. The refractive index of the crude product was 1.4961, this indicating a conversion of 32.6% of the diisopropylbenzene to oxidized materials Analysis of thereaction product showed the presence of 23.3% un-dimethfl-p-iso propylbenzyl hydroperoxide.
. The examples have set forth the use of diisopropylbenacne and p-ethylisopropylbenzene as the compoundsto which the oxidation has been applied, but other com pounds having the structural formula previously set forth for the alkyl-substituted aromatic organic com poundsmay be utilized; Exemplary of such are triiso- P Pylbenzene and p-butylisopropylbenzene. The main requirement for the compounds which may be oxidized in accordance with thisinvention is the presenceof a. tertiary carbon atom carrying a hydrogen atom as its fom'th substituent. As shownby the structural formula the carbon atom is tertiary because it is directly connected to three other carbon atoms contained in the groups rep-- resented by R1, R: and Ar. The alkarvl group need not be derived'from benzene as'is the case' in diisopropylbenzene. Compounds containing aromatic nuclei such as those derived from naphthalene, anthracene and phenanthrene also are operable, but some of. these compounds, being solids, must be dissolved in ,a suitable solvent. such as benzene, during the liquid phase oxidation. The alkaryl group essentiallv is an aromatic nucleus substituted with one or more alkyl groups containing two or more carbon atoms. Representative alkyl groups composing pounds per square inch, the rate of input may be from per hour per kilogram of the alkaryl compound, a pre erable ran being from about $0 to about 280 liters per hour per ograrn.
The oxidation process of this-invention is carried out in the presence of a catalytically active heavy metal compound, particularly of such metals as manganese, cobalt, lead, iron, nickel, copper, vanadium, chromium and mercury. The oxides, hydroxides, or organic acid salts of any of these metals or combinations thereof which are phthalate, manganese linoleate, manganese naphthenate,
. a mixture of manganese and lead acetates, cobalt linoleate,
the alkyl side chain portion of the alkaryl group may be illustrated by the ethyl group in p-ethylisopropylbenzene,
the isopropyl group in p-diisopropylbenzene and the two isopro yl groups in triisopropvlbenzene and the groups may, for. example. be ethyl, propyl. isopropyl. butyl. isobutyl'. secondary butvl, tertiary butyl, and the like. Those compounds containing alkarvl grou s in which the alkyi snbstituent contains, directly attached to the aromatic nucleus. a tertiary carbon atom carrying a hydrogen atom as its fourth substituent. are capable of being oxidized to dihydroperoxides. Illustrative of such compounds is diisopropylbenzene, which may be oxidized to a,a,a',|z'- tetramethyl-p-xvlylene dihydroperoxide. Similarly, compounds containing two tertiary alkvl substituents in the alkaryl group may be oxidized to trihydro eroxides. Exemplary of such compounds is triisopropylbenezene. The alkyl substituents in the .alkaryl groups may, in other words, have the same configuration as the tertiary alkyl' in the structural formula-shown previously The alkyl groups as represented bv R1 and R: in the structural formula need not be limited to the methyl groups of pethylisopropylbenzene and diisopropylbenzene. Other alkyl groups such as those previously indicated as suitable in composing the alkvl substituents of the alkaryl groups may be utilized, and R1 and R: may be either the same or difierent.
The examples have set forth the use of molecular oxygen as the oxygen-containing gas'but air also may be used. The oxygen may be furnished also in mixtures of oxygen with nitrogen or other inert gases. Oxygen, when used alone, may be in the form of pure or commercial oxygen. Air may be utilized either as it is readily available or as humidified up to the saturation point. Furthermore,
it is advisable to wash the air with a caustic solution in order to remove carbon dioxide. The rate of input of the oxygen-containing gas may vary within a wide range,
cobalt naphthenate, mixed lead-cobalt naphthenate, and the heavy metal resinates, such as manganese, lead or cobalt resinate. The resinates may be derived from any rosin acid, such as abietic, piman'c, dehydroabietic, dihydroabietic or tetrahydroabietic acid. 'Ihose oxidized oils obtained according to the process of this invention and containing preponderant amounts of hydroperoxides are useful in initiating the oxidation reaction by relieving inhibitions caused by harmful impurities. 'Ihese oxidized oils, however, do not act as actual catalysts and are therefore highly desirable initiators for those oxidations which exhibit inhibition.
The concentration of the catalytically active heavy metal compound is critical in obtaining high hydroperoxide yields. If the concentration of the catalyst is too low, the reaction is too slow and if the catalyst concentration is higher than the maximum value utilized in accordance 1 with this invention, the yield of hydroperoxide wil be adversely affected. In general, high hydroperoxide yields may be obtained if the concentration of the catalyst in solution in the oxidation reaction mixture is at any particular instant from about 0.15 to about 0.8% based on the alkyl-substituted aromatic organic compound. A preferable range on this basis is from about 0.2 to about 0.6%, and a particularly applicable range is from about 0.25 to about 0.5 Since many of the heavy metals have a tendency to precipitate as peroxides, such as manganese dioxide, from, for example, their salts with organic acids, it may be necessary from time to time to add an additional amount of the catalyst inorder to maintain the desired catalyst concentration. Within the ranges of catalyst concentration, the amount of any particular catalyst will vary somewhat depending upon the metal content and activity of the catalyst. It is possible, for example, in the preparation of the heavy metal salts of organic acids to'vary the amount of metal contained in the final salt, consequently smaller amounts of a salt containing a relatively high metal content will be needed in comparison to the same salt containing a smaller amount of the metal. Similarly the cobalt salts are more active than the manganese and lead salts, and the naphthenates are more active than the linoleates, which in turn are more active than the acetates. Consequently, a smaller amount of cobalt naphthalene, for example, will be needed than will be needed in the case of lead naphthenate or manganese linoleate. Relative to the hydroperoxide-rich oils which may be used to initiate the oxidation reaction, these oils may be used in amounts varying from about I to about 50% based onthe alkyl-substituted aromatic organic gggpound, but a preferable range is from about 2 to about a The temperatures at which the oxidations are carried out also are quite critical in obtaining optimum yields of hydroperoxides. The temperatures which actually may be used,- however, will depend 'on thepressure existing during the oxidations. Upon the basis of atmospheric pressure, the temperature should be in the range of about 40' to about 70' C., a more desirable range being between about and about 65' C., and avparticularly advantageous range being between about and about C. The minimum temperature of 40 C. is necessary since the process of this invention utilizes low catalyst concentrations and the rate of reaction at, for example, room temperature, is too slow to be of commercial signiiicance. On the other hand, if the temperature during oxidation is too high, the reaction occurs in such a manner as to result in excessive ketone formation. In the I case of p-diisopropyl-benzene, for example, oxidation at phenone, consequently the maximum temperature which should be used at atmospheric pressure in order to obtain high yields of hydroperoxides and minimize ketone formation is 70 C.
Temperatures greater than 10 C. may be used, how ever, in the process of this invention providing the pressure is increased to greater than atmospheric. Although elevation of the temperature 'during the oxidation to greater than 70 C. will cause increased decomposition of the hydroperoxides to ketones, this is offset by the in creased rate of hydroperoxide formation caused by the elevation of the pressure. Also, it is possible to hinder the decomposition of the hydroperoxides to ketones, as caused by elevation of the temperature, by using a low activity catalyst such as lead naphthenate or linoleate, and
I by maintaining the catalyst concentration at a low level within the broad ranges of 0.15 to 0.8%. A catalyst concentration between about 0.15 and about 0.3% generallyis satisfactory. In'other words, by proper selection -of pressure, catalyst and catalyst concentration, tempera tures above 70' C. may be used during the oxidation to obtain in shorter lengths of time oxidation reaction products having hydroperoxide and ketone contents as desirable as those reaction products obtained at a temperature of 70? C. or less. The amount of ketone will not be out of proportion to the amount of hydroperoxide.
' Using pressures greaterthan atmospheric the process of this invention therefore may be carried out at temperatures between about 40 and about 140 C., a more desirable range being between about 45 and about 130 C., and a particularly advantageous range between about 50' and about'120 C.
The pressures which can be utilized during those oxidations carried out at greater than atmospheric pressure are limited only by equipment design. From a practical standpoint pressures from atmospheric up to about 500 pounds per square inch are feasible. A preferable range is from about 50 to about 200 pounds per square inch.
Since the reaction is heterogeneous, suitable agitation is necessary. It is particularly important to bring the air, oxygen, or other oxygen-containing gas into intimate con tact with the liquid phase, and this may be effected by using high-speed stirrers, suitable nozzles, porous plates or their combinations.
The course of the reaction may be followed by taking samples at intervals and determining the refractive index of the oily material. In the oxidation of diisopropylbenzene, for example, refractive index values between about 1.4955 and about 1.5030 indicate that about 30 to about 70% of the original organic material has been oxidized, and the reaction then is advisably interrupted. Conversions from about 30 to about 70% can easily be obtained in the process of this invention and it isdesirable in obtaining high hydroperoxide yields to carry the conversion up to about 50-70%, since it generally is not until this conversion value is exceeded that undue amounts of sec- 'ondary products such as the corresponding. alcohol or ketone are formed.
The method utilized in recovery of the reaction products will vary depending upon the use to which the hydroperoxide is to be put. If the use of the hydroperoxide does not require separation of the hydroperoxide from other components, such as alcohols, ketones and unreacted starting material which may be present in the crude reaction mixture, the oily reaction product may be filtered through a layer of some filter aid to remove the catalyst by adsorption, then washed with dilute'aqueous alkali and used either in the wet, slightly cloudy state for various purposes or after clarification and drying by filtration. The dilute aqueous alkali used in the washing step may be sodium hydroxide, sodium carbonate, sodium bicarbonate, and the like, the concentration of these alkalies in aqueous solution ranging from about 1 to about 10%, .but preferably from about 2 to about 5%. If it is desired, however, to obtain a highly concentrated hydroperoxide, the crude reaction product, after the alkali wash, may
be stripped of unreacted hydrocarbon by distillation at pressures of about 1 to about millimeters of mercury per square centimeter. may safel y distilled at temperatures below about 100' C., thus requiring the use, however, of pressures of about 0.01 to about 1.0 Another method of separat- The hydroperoxides themselves formation of secondary 6 ingtheh droperoxldesfmmthecrudeoilyreactionproduct invo ves precipitation of the hydroperoxide with a concentrated aqueous solution ,(25 to ofsodium hydroxide. The precipitate is crystalline and on the basis of analysis is a compound of the hydroperoxide with sodium hydroxide and water.
The oxidation according to this invention apparently roceeds by a peroxide mechanism. Using p-diisopropylnzene as an example, when this com und is oxidized with molecular oxygen, a hydroperoxide is formed on the tertiary carbon atom of one of the isopropyl groups. In the presence of the small amount of catalyst utilized inaccordance with this invention, a very small fraction of the hydroperoxide is decomposed, resulting in the formation of free radicals which are sufficient to initiate the formation of more hydroperoxide molecules. If the concentration of the catalyst exceeds the amount specified in accordance with this invention, increasing. amounts or; hydroperoxide will decompose, resulting in an accelerationof the over-all oxidation, but decreasing the amount of undecomposed hydroperoxide at the expense of the roducts su'chas alcohols and itetones. That the oxidation follows a chain mechanism is shown by the existence of an induction period, by cases of inhibition, and by the fact that both may be eliminated by the addition of hydroperoxide-rich oils from a previous oxidation run. The process of this invention is advantageous in that it has been found possible by proper selection of catalyst concentration and temperature to obtain aryl(dialkyl)- methyl hydroperoxides. These hydroperoxides are highly useful and find various commercial applications. They are excellent catalysts for the polymerization of vinyl, vrnylidene, and vinylene compounds, being, for example, hlghly useful in the copolymerization of butadiene and styrene to form synthetic rubber, and they also are useful in rubber reclaiming, in flotation, and in kier boiling,
bleaching and other textile operations. What we claim and desire to protect by Letters Patent is:
1 The process of preparing a substantial yield of a tertlaryhydroperoxide which comprises passing an oxygen-containing gas through an alkyl-substituted aromatic organic compound having the structural formula r I R: Ar in liquid phase in the presence of a catalyst of the group consisting of heavy metal oxides, hydroxides, organic acid salts and thereof, the concentration of the catalystm solution in the oxidation reaction mixture being from about 0.15 to about 0.8%, based on the alkylsubstituted aromaticcompound, and in the structural formula R1 and R: representing alkyl groups and Ar representing an alkaryl group containing two or more carbon atoms in the alkyl side chain.
2 The process of p aring a substantial yield of a tertiary hydroperoxide w ich comprises passing an oxygen-containing gas through an alkyl-substituted aromatic organic compound having the structural formula Rt H in liquid phase in the an organic isers.
stituted aromatic compound, and in the structural formula R1 and R2 representing alkyl groups and Ar represent-- ing an alkaryl group containing two or more carbon atoms in the alkyl side chain.
4. The process of p aring a substantial yield of a tertiary h xide w ich comprises passing an oxygen-contaming gas through an alkyl-substituted aromatic organic compound having the structural formula Rs Ar in liquid phase in the presence of a heavy metal salt of an organic acid, the concentration of the heavy metal salt in solution in the oxidation. reaction mixturebeing from about 0.25 to about 0.5%, based on the alkyl-substituted aromatic compound, and in the structural formula R1 and R: representing alkyl groups and Ar representing an alkaryl group containing two or more carbon atoms in the alkyl side chain.
5. The process of preparing a substantial yield of a tertiary hydroperoxide which comprises passing an oxygen-containing gas through an alkyl-substituted aromatic compound having the structural formula in liquid phase in the presence of a manganese salt of an organic acid, the concentration. of themanganese salt in solution in the oxidation reaction mixture being from about 0.15 to about 0.8%, based on the alkylsubstituted aromatic compound, and in the structural formula R1 and R: representing alkyl groups and Ar representing an alkaryl group containing two or more carbon atoms in the alkyl side chain.
6. The process of preparing a substantial yield of a tertiary hydroperoxide which comprises passing an oxygen-containing gas through an alkyl-substituted aromatic organic compound having the structural formula in liquid phase in the presence of manganese naphthenate, the concentration of the manganese naphthenate in solution in the oxidation reaction mixture being from about 0.15 to about 0.8%, based on the alkyl-substituted aromatic compound, and in the structural formula R1 and Rz representing alkyl groups and Ar representing an alkaryl group containing two or more carbon atoms in the alkyl side chain.
mmpflgqg .ani diisopropyl t ne in the liquid phase in the presence of a heavy metal salt of an organic acid, the concentration of the heavyfmetal. salt in solution in the oxidation reaction mixture being from about 0.15 to about 0.8%,-based on the, p-diisopropylbenzene.
9. The process of preparing a substantial yield of a,a-
com-
dimethyl -p-isopropylbenzyl hydroperoxide which prises, passing oxygen through pdiisopropylbenzene in the liquid phase in the presence of manganese naphthenate, the concentration of the manganese naphthenate in solution in the oxidation reaction mixture being from.
about 0.15 to about 0.8%, based on the p-diisopropylbenzene.
'10. The process of reparing a substantial yield of ,adimethyl-p-ethylbenzy hydroperoxide which comprises passing an oxygen-containing gas through p-ethylisogropylbenzenein the liquid phase in the presence of a eavy metal salt of an organic acid, the concentration of the heavy metal salt in solution in the oxidation reac-v tion mixture being from about 0.15 to about 0.8%, based on the p-ethylisopropylbenzene.
11. The process of preparing a substantial yield of a, dimethyl-p-ethylbenzyl hydroperoxide which comprises passing oxygen through p-ethylisopropy1benzene in the liquid phase in the presence of cobalt linoleate, the concentration of the cobalt linoleate in solution in the oxidation reaction mixture being from about 0.15 to about 0.8%, based on the p-ethylisopropylbenzene.
12. The process of preparing a substantial yield of ,u,a,'-tetrarnethyl-p-xylylene dihydroperoxide which comprises assing an oxygen-containing gas through pdiisopropyl of the heavy metal salt in solution in the oxidation reaction mixture being from about 0.15 to about 0.8% based on the p-diisopropylbenzene.
13. The process 6 preparing a substantial butylisopropylben'zene hydroperoxide which comprises 7. The process of preparing a s ubstantial yield of a tertiary hydroperoxide which comprises passing oxygen through an alkyl-substituted aromatic organic compound having the structural formula passing an oxygencontaining gas through p-butylisopropylbenzene in the liquid phase in the presence of a heavy metal salt of an organic acid, the concentration of the heavy metal salt in solution in the oxidation reaction mixture being from about 0.15 to about 0.8% based on the 1ributylisopropylbenzene.
14. e process of preparing a substantial yield of triisopropylbenzene trihydroperoxide which comprises passing an oxygen containing gas through triisopropylbenzene in the liquid phase in the presence of a heavy metal salt of an organic acid, the concentration of the heavy metal salt in the solution in the oxidation reaction mixture being from about 0.15 to about 0.8% based on the triisopropylbenzene.
As a new product, trit'sopropylbenzene trihydroperoxide.
Relerenees Clted in the file of this patent or the original patent UNITED STATES PATENTS Number Name Date 2,302,466 Palmer et al. Nov. 17, 1942 2,403,771 Vaughn et al. July 9, 1946 2,430,864 Farkas et a1 Nov. 18, 1947 2,434,888 Rust et al. Jan. 20, 1948 2,548,435 Lorand et al. Apr. 10, 1951 FOREIGN PATENTS Number Count Date 99,523 Switzerlan June 1, 1923 784,016 France Apr. 15, 1935 OTHER REFERENCES Hock et al., Ben, vol 77, pp. 257 to 264 (1944).
an oxygen-containing gas through pnzene in the liquid phase in the presence of a heavy metal salt of an organic acid, the concentration,
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US4503262A (en) 1983-08-04 1985-03-05 Virginia Chemicals, Inc. Process for the production of 2,6-diisopropylnaphthalene dihydroperoxide

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