GB640040A - Improvements in or relating to a process for producing mono-alkylbenzenes and the mono-alkylbenzenes resulting from said process - Google Patents

Improvements in or relating to a process for producing mono-alkylbenzenes and the mono-alkylbenzenes resulting from said process

Info

Publication number
GB640040A
GB640040A GB27132/47A GB2713247A GB640040A GB 640040 A GB640040 A GB 640040A GB 27132/47 A GB27132/47 A GB 27132/47A GB 2713247 A GB2713247 A GB 2713247A GB 640040 A GB640040 A GB 640040A
Authority
GB
United Kingdom
Prior art keywords
alkylator
benzene
liquor
mono
alkyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB27132/47A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Monsanto Chemicals Ltd
Monsanto Chemical Co
Original Assignee
Monsanto Chemicals Ltd
Monsanto Chemical Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Monsanto Chemicals Ltd, Monsanto Chemical Co filed Critical Monsanto Chemicals Ltd
Publication of GB640040A publication Critical patent/GB640040A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/54Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
    • C07C2/64Addition to a carbon atom of a six-membered aromatic ring
    • C07C2/66Catalytic processes
    • C07C2/68Catalytic processes with halides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2527/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • C07C2527/06Halogens; Compounds thereof
    • C07C2527/125Compounds comprising a halogen and scandium, yttrium, aluminium, gallium, indium or thallium
    • C07C2527/126Aluminium chloride
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

Mono-alkyl benzenes are produced by supplying simultaneously and in parallel flow to each of two alkylators 1 and 2 containing alkylation liquor including an aluminium chloride-aromatic hydrocarbon complex, a stream of benzene, introducing to alkylator 2 a gaseous olefin, e.g. ethylene, propylene or butylene, in such an amount as to maintain a reaction temperature of 80-100 DEG C., and to alkylator 1 an amount of said olefin in excess thereof, continuously withdrawing liquor from alkylator 1, cooling, contacting with olefin off gas from 1 and 2, withdrawing alkylated liquor from 1 and 2, separating it into benzene, mono-alkyl, and poly-alkyl benzene fractions, and returning poly-alkyl benzene to alkylator 2. A promoter, e.g. 0.3 per cent hydrogen chloride or ethyl chloride, may be added to the dry benzene. Each alkylator operates at 80-100 DEG C. and substantially atmospheric pressure, and is connected to a separator which separates and returns the catalyst complex. At equilibrium, 10-30 per cent of the total olefin is fed to alkylator 2. The off-gases are scrubbed with cooled reaction liquor, at 40-50 DEG C., with benzene, and finally with poly-alkyl benzene. Alkylate liquor from the separators is water and alkali washed prior to fractionation. Fresh aluminium chloride is added to the circulating complex in both alkylators.
GB27132/47A 1946-11-14 1947-10-09 Improvements in or relating to a process for producing mono-alkylbenzenes and the mono-alkylbenzenes resulting from said process Expired GB640040A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US640040XA 1946-11-14 1946-11-14

Publications (1)

Publication Number Publication Date
GB640040A true GB640040A (en) 1950-07-12

Family

ID=22052921

Family Applications (1)

Application Number Title Priority Date Filing Date
GB27132/47A Expired GB640040A (en) 1946-11-14 1947-10-09 Improvements in or relating to a process for producing mono-alkylbenzenes and the mono-alkylbenzenes resulting from said process

Country Status (1)

Country Link
GB (1) GB640040A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3255269A (en) * 1965-02-05 1966-06-07 Halcon International Inc Process for preparation of ethylbenzene
JPS5092297A (en) * 1973-12-12 1975-07-23

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3255269A (en) * 1965-02-05 1966-06-07 Halcon International Inc Process for preparation of ethylbenzene
JPS5092297A (en) * 1973-12-12 1975-07-23
JPS562050B2 (en) * 1973-12-12 1981-01-17

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