GB1285133A - Production of carboxylates of neo-alcohols - Google Patents
Production of carboxylates of neo-alcoholsInfo
- Publication number
- GB1285133A GB1285133A GB2031770A GB2031770A GB1285133A GB 1285133 A GB1285133 A GB 1285133A GB 2031770 A GB2031770 A GB 2031770A GB 2031770 A GB2031770 A GB 2031770A GB 1285133 A GB1285133 A GB 1285133A
- Authority
- GB
- United Kingdom
- Prior art keywords
- neo
- alkyl
- carboxylates
- alkenyl
- isobutyrate
- 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
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/22—Esters 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
- C07C69/24—Esters 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1285133 Neo-alkyl carboxylates BP CHEMICAL Ltd 19 April 1971 [28 April 1970] 20317/70 Heading C2C Neo-alkyl carboxylates are prepared by hydrogenating a neo-alkenyl carboxylate by trickling it over a Group IB or VIII metal hydrogenation catalyst on an inert support in an atmosphere of hydrogen. By "neo-alkyl" and "neo-alkenyl" is meant an alkyl or alkenyl group in which the #-carbon atom is linked only to carbon atoms. The hydrogenation is preferably carried out at a temperature not exceeding 250‹ C. under a pressure below 250 p.s.i.g. Examples describe the conversion of 2,2,4-trimethylpentenyl - 1 - isobutyrate to 2,2,4 - trimethylpentyl-1-isobutyrate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2031770A GB1285133A (en) | 1970-04-28 | 1970-04-28 | Production of carboxylates of neo-alcohols |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2031770A GB1285133A (en) | 1970-04-28 | 1970-04-28 | Production of carboxylates of neo-alcohols |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1285133A true GB1285133A (en) | 1972-08-09 |
Family
ID=10143967
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2031770A Expired GB1285133A (en) | 1970-04-28 | 1970-04-28 | Production of carboxylates of neo-alcohols |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1285133A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0317975A2 (en) * | 1987-11-25 | 1989-05-31 | Union Carbide Corporation | Process for the production of saturated neo-alcohols |
-
1970
- 1970-04-28 GB GB2031770A patent/GB1285133A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0317975A2 (en) * | 1987-11-25 | 1989-05-31 | Union Carbide Corporation | Process for the production of saturated neo-alcohols |
EP0317975A3 (en) * | 1987-11-25 | 1990-05-16 | Union Carbide Corporation | Process for the production of saturated neo-alcohols |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |