GB639873A - 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
GB639873A
GB639873A GB27005/47A GB2700547A GB639873A GB 639873 A GB639873 A GB 639873A GB 27005/47 A GB27005/47 A GB 27005/47A GB 2700547 A GB2700547 A GB 2700547A GB 639873 A GB639873 A GB 639873A
Authority
GB
United Kingdom
Prior art keywords
benzene
alkylator
mono
ethylene
returned
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
GB27005/47A
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 GB639873A publication Critical patent/GB639873A/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

Landscapes

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

Abstract

Mono-alkyl benzenes are prepared by mixing benzene and a gaseous olefin in the presence of a Friedel-Crafts' catalyst at a pressure sufficient to maintain the liquid phase and at a temperature of 100-200 DEG , preferably 150-200 DEG C., and then passing the product to an evaporation zone at a lower pressure wherein lower boiling constituents are evaporated. Dry benzene, ethylene and aluminium chloride may be fed to an alkylator, the temperature rising, say, to 163 DEG C., and the pressure to 100-200, e.g. 150 p.s.i. The reaction liquor is then passed through an expansion valve to a flash column at about 1 p.s.i., benzene being vaporized, condensed and returned in part as reflux and in part to the alkylator. The bottoms from the column at about 115 DEG C. may be in part returned to the alkylator and in part to a separator where catalyst complex is separated and returned to the alkylator, except for a part used to dealkylate the poly-ethyl benzene. The separated alkylate is cooled to 20-30 DEG C., and further separated from complex. Polyethyl benzene, benzene and ethylene, in the presence of complex, are treated in a dealkylator giving a further conversion to ethyl benzene. Off-gases of the process comprising ethylene, ethyl chloride, hydrogen chloride and some benzene are treated in an absorber with polyethyl benzene prior to feeding the latter to the dealkylator.
GB27005/47A 1946-11-14 1947-10-08 Improvements in or relating to a process for producing mono-alkylbenzenes and the mono-alkylbenzenes resulting from said process Expired GB639873A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US639873XA 1946-11-14 1946-11-14

Publications (1)

Publication Number Publication Date
GB639873A true GB639873A (en) 1950-07-05

Family

ID=22052792

Family Applications (1)

Application Number Title Priority Date Filing Date
GB27005/47A Expired GB639873A (en) 1946-11-14 1947-10-08 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) GB639873A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5092297A (en) * 1973-12-12 1975-07-23
EP0050222A1 (en) * 1980-10-22 1982-04-28 BASF Aktiengesellschaft Process for the continuous preparation of ethylbenzene in the heterogeneous phase
EP0190057A1 (en) * 1985-01-31 1986-08-06 The Dow Chemical Company Process for the alkylation of aromatic hydrocarbons

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5092297A (en) * 1973-12-12 1975-07-23
JPS562050B2 (en) * 1973-12-12 1981-01-17
EP0050222A1 (en) * 1980-10-22 1982-04-28 BASF Aktiengesellschaft Process for the continuous preparation of ethylbenzene in the heterogeneous phase
US4431854A (en) * 1980-10-22 1984-02-14 Basf Aktiengesellschaft Continuous preparation of ethylbenzene in a heterogeneous-phase reaction
EP0190057A1 (en) * 1985-01-31 1986-08-06 The Dow Chemical Company Process for the alkylation of aromatic hydrocarbons

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