GB583720A - Manufacture of new aminotriazines - Google Patents
Manufacture of new aminotriazinesInfo
- Publication number
- GB583720A GB583720A GB23200/44A GB2320044A GB583720A GB 583720 A GB583720 A GB 583720A GB 23200/44 A GB23200/44 A GB 23200/44A GB 2320044 A GB2320044 A GB 2320044A GB 583720 A GB583720 A GB 583720A
- Authority
- GB
- United Kingdom
- Prior art keywords
- heating
- carbon atoms
- sulphuric acid
- cyanohydrin
- group preferably
- 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
- Adhesives Or Adhesive Processes (AREA)
Abstract
Amino-triazines of the formula <FORM:0583720/IV/1> in which R is an alkoxy group preferably containing 1 to 4 carbon atoms or an alkoxyalkoxy group preferably containing from 2 to 8 carbon atoms, and R1 is hydrogen or an alkyl group preferably containing 1 to 3 carbon atoms, are obtained by heating (e.g. to 150-200 DEG C.) dicyandiamide with a nitrile of the formula R.CH(R1)CN, preferably in the presence of an alkaline reacting material, e.g. piperidine. The reaction may be carried out at atmospheric pressure or in any suitable pressure-resisting vessel. In examples, dicyandiamide is heated with (1) ethoxymethoxyacetonitrile; (2) isobutoxymethoxyacetonitrile; (3) tert-butoxyacetonitrile. Other specified nitriles are methoxymethoxyacetonitrile, methoxyaceto - nitrile, a -methoxypropionitrile and a -ethoxymethoxypropionitrile. Synthetic resins are obtained by condensing the above compounds with formaldehyde or with reactive urea-formaldehyde condensation products, e.g. dimethylol urea. These resins are useful for the manufacture of moulded articles, impregnated paper and wood, coatings, electrical insulation and adhesives, particularly plywood adhesives. Methoxymethoxyacetonitrile and ethoxymethoxyacetonitrile are obtained by heating formaldehyde cyanohydrin with methylal and diethyl formal respectively in the presence of sulphuric acid. a -Ethoxymethoxypropionitrile is obtained by heating acetaldehyde cyanohydrin and diethyl formal in the presence of sulphuric acid. Iso-butoxymethoxyacetonitrile is obtained by heating iso-butyraldehyde cyanohydrin and methylal in the presence of sulphuric acid. Tertiary-butoxyacetonitrile is obtained from t-butyl ether and cuprous cyanide.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US583720XA | 1943-11-23 | 1943-11-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB583720A true GB583720A (en) | 1946-12-30 |
Family
ID=22016408
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB23200/44A Expired GB583720A (en) | 1943-11-23 | 1944-11-22 | Manufacture of new aminotriazines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB583720A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2857382A (en) * | 1956-03-02 | 1958-10-21 | Rohm & Haas | Guanamine derivatives |
-
1944
- 1944-11-22 GB GB23200/44A patent/GB583720A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2857382A (en) * | 1956-03-02 | 1958-10-21 | Rohm & Haas | Guanamine derivatives |
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