GB743463A - Process for producing isopropyl esters - Google Patents

Process for producing isopropyl esters

Info

Publication number
GB743463A
GB743463A GB33663/53A GB3366353A GB743463A GB 743463 A GB743463 A GB 743463A GB 33663/53 A GB33663/53 A GB 33663/53A GB 3366353 A GB3366353 A GB 3366353A GB 743463 A GB743463 A GB 743463A
Authority
GB
United Kingdom
Prior art keywords
acid
reaction mixture
per cent
weight
isopropyl ester
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
GB33663/53A
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.)
Usines de Melle SA
Original Assignee
Usines de Melle SA
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 Usines de Melle SA filed Critical Usines de Melle SA
Publication of GB743463A publication Critical patent/GB743463A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/02Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
    • C07C69/22Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety
    • C07C69/24Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety esterified with monohydroxylic compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/04Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/02Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
    • C07C69/22Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety

Landscapes

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

Abstract

An isopropyl ester of an aliphatic acid containing from 2 to 8 carbon atoms is produced by a continuous process comprising maintaining at a temperature of from 60 DEG to 80 DEG C. a reaction mixture having the following composition :-strong mineral acid 15-30 per cent by weight, aliphatic acid 5-30 per cent by weight, the isopropyl ester of the aliphatic acid 5-10 per cent by weight, water 0.5-11 per cent by weight, the remainder being an isopropyl ester of the mineral acid, feeding the reaction mixture with the aliphatic acid at a rate sufficient to maintain the proportion thereof within the range stated above, continuously passing a gas containing at least 30 per cent by volume of propylene through the reaction mixture at a rate of from 2 to 5 cubic metres of gas per hour per kilogram of the reaction mixture, thereby providing an excess of propylene-containing gas sufficient to remove from the reaction mixture the isopropyl ester of the aliphatic acid as rapidly as it is produced. The preferred mineral acid is sulphuric acid. In the examples the isopropyl esters of (a) acetic acid, (b) butyric acid, and (c) octanoic acid are prepared by the process of the invention. U.S.A. Specification 2,079,652 is referred to.
GB33663/53A 1952-12-05 1953-12-03 Process for producing isopropyl esters Expired GB743463A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR1068204T 1952-12-05

Publications (1)

Publication Number Publication Date
GB743463A true GB743463A (en) 1956-01-18

Family

ID=9603580

Family Applications (1)

Application Number Title Priority Date Filing Date
GB33663/53A Expired GB743463A (en) 1952-12-05 1953-12-03 Process for producing isopropyl esters

Country Status (6)

Country Link
US (1) US2740800A (en)
BE (1) BE524866A (en)
DE (1) DE949823C (en)
FR (1) FR1068204A (en)
GB (1) GB743463A (en)
NL (1) NL87452C (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5384426A (en) * 1992-12-08 1995-01-24 Daicel Chemical Industries, Ltd. Process for the preparation of isopropyl acetate

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2079652A (en) * 1934-03-09 1937-05-11 Socony Vacuum Oil Co Inc Manufacture of esters from olefines

Also Published As

Publication number Publication date
US2740800A (en) 1956-04-03
FR1068204A (en) 1954-06-23
DE949823C (en) 1956-09-27
NL87452C (en) 1958-02-15
BE524866A (en) 1954-06-05

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