GB398527A - Manufacture of esters - Google Patents
Manufacture of estersInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/04—Preparation 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.
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)
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 |
-
1932
- 1932-03-08 GB GB688732A patent/GB398527A/en not_active Expired
-
1933
- 1933-03-06 FR FR752008D patent/FR752008A/en not_active Expired
Cited By (2)
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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