GB494666A - Process of preparing monohydric alcohols - Google Patents
Process of preparing monohydric alcoholsInfo
- Publication number
- GB494666A GB494666A GB862537A GB862537A GB494666A GB 494666 A GB494666 A GB 494666A GB 862537 A GB862537 A GB 862537A GB 862537 A GB862537 A GB 862537A GB 494666 A GB494666 A GB 494666A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mixture
- nitriles
- carbon atoms
- acid solution
- separated
- 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
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/09—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Aliphatic monohydric alcohols are made by hydrogenating a nitrile or mixture of nitriles having six or more carbon atoms to produce the amine while in acid solution, using a platinum catalyst, and then treating with a nitrite. The alcohols produced may have 6-19 carbon atoms or more, and may be saturated or unsaturated. In an example, lauronitrile is hydrogenated in hydrochloric, sulphuric, glacial acetic or acetic acid solution with a platinum catalyst, ethyl alcohol being added as a solvent. To the reaction product is added more ethyl alcohol and sodium nitrite. After the reaction an alcoholic layer is separated and the product is washed with acidified aqueous alcohol and then with hot water. When the initial material is a mixture of nitriles the mixture of alcohols produced may be separated by fractional distillation under reduced pressure. Specifications 467,043, 467,044, and 477,463 are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB862537A GB494666A (en) | 1937-03-24 | 1937-03-24 | Process of preparing monohydric alcohols |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB862537A GB494666A (en) | 1937-03-24 | 1937-03-24 | Process of preparing monohydric alcohols |
Publications (1)
Publication Number | Publication Date |
---|---|
GB494666A true GB494666A (en) | 1938-10-24 |
Family
ID=9856064
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB862537A Expired GB494666A (en) | 1937-03-24 | 1937-03-24 | Process of preparing monohydric alcohols |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB494666A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2978516A (en) * | 1953-12-08 | 1961-04-04 | Aerojet General Co | Alcohols |
US3714270A (en) * | 1970-06-24 | 1973-01-30 | Union Oil Co | Hydration of amines to alcohols |
-
1937
- 1937-03-24 GB GB862537A patent/GB494666A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2978516A (en) * | 1953-12-08 | 1961-04-04 | Aerojet General Co | Alcohols |
US3714270A (en) * | 1970-06-24 | 1973-01-30 | Union Oil Co | Hydration of amines to alcohols |
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