GB812780A - Process for preparing alkene nitriles - Google Patents
Process for preparing alkene nitrilesInfo
- Publication number
- GB812780A GB812780A GB39314/56A GB3931456A GB812780A GB 812780 A GB812780 A GB 812780A GB 39314/56 A GB39314/56 A GB 39314/56A GB 3931456 A GB3931456 A GB 3931456A GB 812780 A GB812780 A GB 812780A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cyano
- per cent
- catalyst
- vapour
- lactam
- 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
- C07C255/00—Carboxylic acid nitriles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Unsaturated aliphatic nitriles are obtained by the vapour phase reaction at 250-450 DEG , preferably about 350-400 DEG C., of a lactam with a molar excess of ammonia over a dehydration catalyst which is acidic in water. The ammonia may be present in amounts of 5 to 15 mols. per mol. of lactam. The dehydration catalyst, e.g. acid-treated clay, boron phosphate, or phosphoric acid on a carrier such as kieselguhr, fuller's earth or silica, is preferably used in the form of irregular lumps with a mean diameter of 5-6 mm. The vapour is passed through the catalyst mass. The pressure is about atmospheric, and may be from about 0.5 atm. to 1.5 atm., i.e. sufficient to draw or force the vapour through the catalyst. In an example caprolactam is 91.8 per cent converted to a mixture of 91 per cent 5-cyano pentene-1, 8 per cent aminocapronitrile and 1 per cent high-boiling residue. The nitrile reaction product is purified by distillation. Suitable lactams mentioned as starting materials are caprylolactam, 2-pyrrolidene, valerolactam and oenantholactam, giving respectively 7-cyanoheptene-1,3-cyano - propene - 1,4 - cyano - butene - 1 and 6-cyano-hexene-1.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL812780X | 1955-12-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB812780A true GB812780A (en) | 1959-04-29 |
Family
ID=19838756
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB39314/56A Expired GB812780A (en) | 1955-12-30 | 1956-12-27 | Process for preparing alkene nitriles |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB812780A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3121733A (en) * | 1958-08-22 | 1964-02-18 | Basf Ag | Production of carboxylic acid nitriles from lactones |
CN116603567A (en) * | 2023-03-27 | 2023-08-18 | 湖北兴发化工集团股份有限公司 | Catalyst for synthesizing 6-aminocapronitrile and preparation method and application thereof |
-
1956
- 1956-12-27 GB GB39314/56A patent/GB812780A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3121733A (en) * | 1958-08-22 | 1964-02-18 | Basf Ag | Production of carboxylic acid nitriles from lactones |
CN116603567A (en) * | 2023-03-27 | 2023-08-18 | 湖北兴发化工集团股份有限公司 | Catalyst for synthesizing 6-aminocapronitrile and preparation method and application thereof |
CN116603567B (en) * | 2023-03-27 | 2024-05-17 | 湖北兴发化工集团股份有限公司 | Catalyst for synthesizing 6-aminocapronitrile and preparation method and application thereof |
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