GB416007A - Improvements in or relating to the manufacture of cyanhydrins - Google Patents
Improvements in or relating to the manufacture of cyanhydrinsInfo
- Publication number
- GB416007A GB416007A GB630333A GB630333A GB416007A GB 416007 A GB416007 A GB 416007A GB 630333 A GB630333 A GB 630333A GB 630333 A GB630333 A GB 630333A GB 416007 A GB416007 A GB 416007A
- Authority
- GB
- United Kingdom
- Prior art keywords
- pyridine
- added
- base
- followed
- dehydrating agent
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Ketone cyanhydrins of the aliphatic series are manufactured by adding to an aliphatic ketone, maintained at boiling point and containing a base dissolved therein, an equimolecular proportion of hydrocyanic acid in the gaseous or, preferably, in the liquid state. Suitable bases are: alcoholic or aqueous caustic soda, gaseous or aqueous ammonia, pyridine, piperidine, quinoline, primary, secondary or tertiary amines, potassium or sodium cyanide. The cyanhydrin is recovered by acidification, preferably with a non-volatile mineral acid, e.g. sulphuric acid, which may be in 50 per cent excess over the base present, followed by distillation under reduced pressure. The cyanhydrins may be converted into unsaturated nitriles of homologues of acrylic acid by dehydration with a powerful dehydrating agent, e.g. phosphorus pentoxide, in the presence of a soluble base, preferably in the presence of a diluent, e.g. tetrahydronaphthalene, which may be added before or after the dehydrating agent. The dehydrating agent may be added to the mixture of cyanhydrin and base with efficient cooling, or the dehydrating agent may be added first followed by the base. In examples: (1) liquid hydrocyanic acid is added to a boiling solution of piperidine in acetone and the acetone cyanhydrin is isolated and converted to methacrylonitrile by adding quinoline followed by phosphorus pentoxide, if desired with the addition of a diluent, e.g. tetrahydronaphthalene; (2) hydrocyanic acid is added to a boiling solution of pyridine in acetone and the reaction mixture is cooled and worked up for the production of methacrylonitrile by the addition of pyridine followed by gradual addition of phosphorus pentoxide and then of more pyridine, or by the addition first of the phosphorus pentoxide and then of the pyridine.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB630333A GB416007A (en) | 1933-03-01 | 1933-03-01 | Improvements in or relating to the manufacture of cyanhydrins |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB630333A GB416007A (en) | 1933-03-01 | 1933-03-01 | Improvements in or relating to the manufacture of cyanhydrins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB416007A true GB416007A (en) | 1934-09-03 |
Family
ID=9812030
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB630333A Expired GB416007A (en) | 1933-03-01 | 1933-03-01 | Improvements in or relating to the manufacture of cyanhydrins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB416007A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2441462A (en) * | 1946-03-05 | 1948-05-11 | American Cyanamid Co | Preparation of alpha-methacrylonitrile |
US2500403A (en) * | 1940-07-23 | 1950-03-14 | American Cyanamid Co | Production of olefinic nitriles |
US2558785A (en) * | 1949-02-18 | 1951-07-03 | Merck & Co Inc | 20-cyanopregnenes and process |
US6743938B1 (en) * | 1999-07-29 | 2004-06-01 | Atofina | Method for making ethyl ketone cyanohydrin |
-
1933
- 1933-03-01 GB GB630333A patent/GB416007A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2500403A (en) * | 1940-07-23 | 1950-03-14 | American Cyanamid Co | Production of olefinic nitriles |
US2441462A (en) * | 1946-03-05 | 1948-05-11 | American Cyanamid Co | Preparation of alpha-methacrylonitrile |
US2558785A (en) * | 1949-02-18 | 1951-07-03 | Merck & Co Inc | 20-cyanopregnenes and process |
US6743938B1 (en) * | 1999-07-29 | 2004-06-01 | Atofina | Method for making ethyl ketone cyanohydrin |
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