GB890526A - Process for the preparation of acrylonitrile - Google Patents
Process for the preparation of acrylonitrileInfo
- Publication number
- GB890526A GB890526A GB29997/59A GB2999759A GB890526A GB 890526 A GB890526 A GB 890526A GB 29997/59 A GB29997/59 A GB 29997/59A GB 2999759 A GB2999759 A GB 2999759A GB 890526 A GB890526 A GB 890526A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acetylene
- hcn
- acrylonitrile
- preparation
- cyanbutadiene
- 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
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/08—Preparation of carboxylic acid nitriles by addition of hydrogen cyanide or salts thereof to unsaturated compounds
- C07C253/12—Preparation of carboxylic acid nitriles by addition of hydrogen cyanide or salts thereof to unsaturated compounds to compounds containing carbon-to-carbon triple bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
The process of the parent Specification for the simultaneous preparation of acrylonitrile, monovinyl acetylene and acetaldehyde by introducing acetylene and hydrocyanic acid under superatmospheric pressure in the range 1-4 atmospheres absolute and at about 70 DEG C. to about 110 DEG C. into an aqueous cuprous chloride solution containing dissolved hydrochloric acid, ammonium chloride and/or an alkali metal chloride is modified by using an amount of between about 20% and 50% of HCN, calculated on that quantity of HCN which would, when using an excess of HCN, be converted to acrylonitrile under the reaction conditions. By-products obtained include divinyl acetylene, cyanbutadiene, methyl vinyl ketone, chloroprene and higher acetylene polymers.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE890526X | 1958-09-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB890526A true GB890526A (en) | 1962-03-07 |
Family
ID=6838692
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB29997/59A Expired GB890526A (en) | 1958-09-09 | 1959-09-02 | Process for the preparation of acrylonitrile |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB890526A (en) |
-
1959
- 1959-09-02 GB GB29997/59A patent/GB890526A/en not_active Expired
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