GB544421A - Improvements in or relating to aliphatic oxy nitriles and methods of preparing the same - Google Patents
Improvements in or relating to aliphatic oxy nitriles and methods of preparing the sameInfo
- Publication number
- GB544421A GB544421A GB15876/40A GB1587640A GB544421A GB 544421 A GB544421 A GB 544421A GB 15876/40 A GB15876/40 A GB 15876/40A GB 1587640 A GB1587640 A GB 1587640A GB 544421 A GB544421 A GB 544421A
- Authority
- GB
- United Kingdom
- Prior art keywords
- product
- nitriles
- relating
- preparing
- methods
- 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
Landscapes
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
544,421. Alkoxynitriles. AMERICAN CYANAMID CO. Oct. 30, 1940, Nos. 15876, 15877 and 15878. Convention dates, Nov. 13, 1939, Nov. 24, 1939, and Aug. 10, 1940. [Class 2 (iii)] Alkoxynitriles are made by re-acting an aliphatic alcohol with a nitrile containing tne | group C =C-C =N in the presence of a soluble | | alkaline catalyst many of which are specified. In examples acrylonitrile is re-acted with methyl, allyl, isopropyl, butyl, tertiary butyl, amyl, 2-ethyl hexyl, dodecyl, and octadecyl alcohols, ethylene cyanhydrin (in which case the product is NC-CH 2 -CH 2 -O-CH 2 CH 2 - ON), and ethylene glycol (in which case the product is NC-CH 2 -CH 2 -O-CH 2 CH 2 -O -CH 2 -CH 2 -CN), and crotonic nitrile is re-acted with ethyl alcohol, the product being
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US544421XA | 1939-11-13 | 1939-11-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB544421A true GB544421A (en) | 1942-04-13 |
Family
ID=21991088
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB15876/40A Expired GB544421A (en) | 1939-11-13 | 1940-10-30 | Improvements in or relating to aliphatic oxy nitriles and methods of preparing the same |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB544421A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2425615A (en) * | 1945-10-03 | 1947-08-12 | Du Pont | Preparation of tertiary alkoxy acetonitriles |
| US2435869A (en) * | 1944-04-19 | 1948-02-10 | Resinous Prod & Chemical Co | Cyanoethylated formals and method for their preparation |
| US2495214A (en) * | 1944-06-02 | 1950-01-24 | Armour & Co | Cyanoether esters of dihydric alcohols |
| US2980698A (en) * | 1958-04-25 | 1961-04-18 | Du Pont | Dicyanoketene cyclic acetals and process for preparation |
| US3253040A (en) * | 1962-12-10 | 1966-05-24 | Union Carbide Corp | Process for the production of primary 3-hydrocarbyloxypropylamines |
-
1940
- 1940-10-30 GB GB15876/40A patent/GB544421A/en not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2435869A (en) * | 1944-04-19 | 1948-02-10 | Resinous Prod & Chemical Co | Cyanoethylated formals and method for their preparation |
| US2495214A (en) * | 1944-06-02 | 1950-01-24 | Armour & Co | Cyanoether esters of dihydric alcohols |
| US2425615A (en) * | 1945-10-03 | 1947-08-12 | Du Pont | Preparation of tertiary alkoxy acetonitriles |
| US2980698A (en) * | 1958-04-25 | 1961-04-18 | Du Pont | Dicyanoketene cyclic acetals and process for preparation |
| US3253040A (en) * | 1962-12-10 | 1966-05-24 | Union Carbide Corp | Process for the production of primary 3-hydrocarbyloxypropylamines |
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