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GB583720A - Manufacture of new aminotriazines - Google Patents

Manufacture of new aminotriazines

Info

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
Application number
GB23200/44A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB583720A publication Critical patent/GB583720A/en
Expired legal-status Critical Current

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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.
GB23200/44A 1943-11-23 1944-11-22 Manufacture of new aminotriazines Expired GB583720A (en)

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)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2857382A (en) * 1956-03-02 1958-10-21 Rohm & Haas Guanamine derivatives

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2857382A (en) * 1956-03-02 1958-10-21 Rohm & Haas Guanamine derivatives

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