GB398527A - Manufacture of esters - Google Patents

Manufacture of esters

Info

Publication number
GB398527A
GB398527A GB688732A GB688732A GB398527A GB 398527 A GB398527 A GB 398527A GB 688732 A GB688732 A GB 688732A GB 688732 A GB688732 A GB 688732A GB 398527 A GB398527 A GB 398527A
Authority
GB
United Kingdom
Prior art keywords
acid
per cent
acids
ester
catalyst
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
GB688732A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to GB688732A priority Critical patent/GB398527A/en
Priority to FR752008D priority patent/FR752008A/en
Publication of GB398527A publication Critical patent/GB398527A/en
Expired legal-status Critical Current

Links

Classifications

    • 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

Landscapes

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

Abstract

Esters are produced by reacting a fatty acid having five or less carbon atoms with an olefine having seven or less carbon atoms in presence of a catalyst at above the boiling-point of the ester under the reaction conditions and continuously withdrawing the ester from the reaction space in the vapour form. When the ester has a higher boiling-point than the acid, the acid must be employed in the form of vapour, but otherwise the acid may be in the liquid form. Suitable catalysts are chlorides, bromides, phosphates and sulphates of zinc, aluminium, mercury, copper, cadmium, bismuth and antimony, relatively non-volatile inorganic acids such as sulphuric and phosphoric acids, and the metal acid salts and alkyl and aryl derivatives of these acids, such as sodium bisulphate, ethyl sulphuric acid, and benzene sulphonic acid. A porous or adsorbent carrier may be used for the catalyst. Reduced, normal, or increased pressure may be employed. Preferably the temperature is as little above the boiling-point of the ester as will ensure the quick removal of the vapour from the reaction space. The excess reagents may be passed through a number of reaction vessels until substantially the whole have combined. In examples, (1) 500 parts adsorbent carbon are treated with 50 parts of 75 per cent phosphoric acid and heated to 150-250 DEG C. for two hours in a current of air, and a mixture of acetic acid vapour and propylene is passed over this catalyst at 110 DEG C.; (2) adsorbent carbon is treated with 10 per cent of a 50 per cent solution of zinc chloride and heated as before, the production of ester being effected in a similar manner. Specification 362,215 is referred to.ALSO:Catalysts for the production of esters from fatty acids and olefines are chlorides, bromides, phosphates and sulphates of zinc, aluminium, mercury, copper, cadmium, bismuth and antimony, relatively non-volatile inorganic acids such as phosphoric and sulphuric acids, and the metal acid salts and alkyl and aryl derivatives of these acids, such as sodium bisulphate, ethyl hydrogen sulphate, and benzene sulphonic acid. A porous or adsorbent carrier may be used for the catalyst. In the examples, catalysts are prepared by treating 500 parts of adsorbent carbon with 50 parts of 75 per cent phosphoric acid or 10 per cent of 50 per cent solution of zinc chloride, the mass being heated for two hours at 150-250 DEG C. in a current of air. Specification 362,215, [Group IV], is referred to.
GB688732A 1932-03-08 1932-03-08 Manufacture of esters Expired GB398527A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB688732A GB398527A (en) 1932-03-08 1932-03-08 Manufacture of esters
FR752008D FR752008A (en) 1932-03-08 1933-03-06 Manufacturing process for esters starting from olefins and monobasic acids from the methane series

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB688732A GB398527A (en) 1932-03-08 1932-03-08 Manufacture of esters

Publications (1)

Publication Number Publication Date
GB398527A true GB398527A (en) 1933-09-08

Family

ID=9822598

Family Applications (1)

Application Number Title Priority Date Filing Date
GB688732A Expired GB398527A (en) 1932-03-08 1932-03-08 Manufacture of esters

Country Status (2)

Country Link
FR (1) FR752008A (en)
GB (1) GB398527A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112920013A (en) * 2021-02-05 2021-06-08 广西壮族自治区林业科学研究院 Turpentine synthesized fatty acid borneol ester, preparation method and application thereof in preparation of borneol

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112920013A (en) * 2021-02-05 2021-06-08 广西壮族自治区林业科学研究院 Turpentine synthesized fatty acid borneol ester, preparation method and application thereof in preparation of borneol
CN112920013B (en) * 2021-02-05 2023-04-07 广西壮族自治区林业科学研究院 Turpentine synthesized fatty acid borneol ester, preparation method and application thereof in preparation of borneol

Also Published As

Publication number Publication date
FR752008A (en) 1933-09-15

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