GB897275A - Production of acrylonitrile cyclic dimer - Google Patents
Production of acrylonitrile cyclic dimerInfo
- Publication number
- GB897275A GB897275A GB41938/60A GB4193860A GB897275A GB 897275 A GB897275 A GB 897275A GB 41938/60 A GB41938/60 A GB 41938/60A GB 4193860 A GB4193860 A GB 4193860A GB 897275 A GB897275 A GB 897275A
- Authority
- GB
- United Kingdom
- Prior art keywords
- water
- acrylonitrile
- less
- pressure
- prepared
- 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
Acrylonitrile cyclic dimers are prepared by heating acrylonitrile in the vapour phase at a pressure of at least 1000 p.s.i. out of contact with stainless steel, copper, or any other non-noble metal and/or in the presence of water at a pH of less than 8. The process may be carried out in a platinum-, glass- or silver-lined pressure-resistant vessel, in the presence or absence of water at a pH of less than 8; or in any suitable vessel in the presence of water at a pH of less than 8. The acidity may be provided by the presence of water-soluble amine acceptors, such as CO2, sulphuric, phosphoric and sulphurous acids, potassium hydrogen phosphates, oxalic, hydroxyacetic, trimethylacetic, propionic, butyric, succinic, acrylic and acetic acids, and water-soluble phenols. The preferred quantity of water is 0.3%-10% based on the acrylonitrile charged. Adiponitrile may be prepared by hydrogenation of acrylonitrile cyclic dimers at atmospheric pressure at 175 DEG C.-400 DEG C. in the presence of a reduced cobalt oxide catalyst.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US897275XA | 1959-12-07 | 1959-12-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB897275A true GB897275A (en) | 1962-05-23 |
Family
ID=22219301
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB41938/60A Expired GB897275A (en) | 1959-12-07 | 1960-12-06 | Production of acrylonitrile cyclic dimer |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB897275A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3202697A (en) * | 1963-06-21 | 1965-08-24 | Standard Oil Co | Process for making cyclobutane-1, 2-dicyanide from acrylonitrile |
US3316288A (en) * | 1963-06-06 | 1967-04-25 | Knapsack Ag | Process for the manufacture of 1, 2-dicyanocyclobutane |
-
1960
- 1960-12-06 GB GB41938/60A patent/GB897275A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3316288A (en) * | 1963-06-06 | 1967-04-25 | Knapsack Ag | Process for the manufacture of 1, 2-dicyanocyclobutane |
US3202697A (en) * | 1963-06-21 | 1965-08-24 | Standard Oil Co | Process for making cyclobutane-1, 2-dicyanide from acrylonitrile |
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