GB639218A - Process for the preparation of diaminotriazines - Google Patents
Process for the preparation of diaminotriazinesInfo
- Publication number
- GB639218A GB639218A GB18996/47A GB1899647A GB639218A GB 639218 A GB639218 A GB 639218A GB 18996/47 A GB18996/47 A GB 18996/47A GB 1899647 A GB1899647 A GB 1899647A GB 639218 A GB639218 A GB 639218A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dicyandiamide
- ammonium
- mol
- heating
- diaminotriazine
- 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
- C07C277/00—Preparation of guanidine or its derivatives, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C277/02—Preparation of guanidine or its derivatives, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups of guanidine from cyanamide, calcium cyanamide or dicyandiamides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Diaminotriazines are manufactured by heating dicyandiamide with a guanidine salt of an organic carboxylic acid at temperatures adjacent to the melting point of dicyandiamide. The guanidine salt may be prepared by heating an ammonium salt of the organic carboxylic acid with dicyandiamide in the presence of an ammonium carbonate, and this preparation and the conversion to a diaminotriazine may constitute two phases of the same operation, consisting in heating an ammonium salt of the organic carboxylic acid with 5-15 per cent excess of dicyandiamide in the presence of an ammonium carbonate. The acid may be alkyl, aryl or aralkyl, substituted or not, and the third carbon atom of the triazine ring will correspondingly bear no substituent or an alkyl, aryl or aralkyl group. In examples: (1) 1 mol. of ammonium acetate and 1/2 mol. of dicyandiamide are heated with 1/4 mol. of ammonium carbonate, then a further 1 mol. of dicyandiamide is added and heating continued at 180-215 DEG C., producing methyl-diaminotriazine; (2) commercially pure butyric acid is heated with excess of ammonium sesquicarbonate and the product is heated with dicyandiamide to give propyl diaminotriazine.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR639218X | 1946-07-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB639218A true GB639218A (en) | 1950-06-21 |
Family
ID=8996607
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB18996/47A Expired GB639218A (en) | 1946-07-16 | 1947-07-16 | Process for the preparation of diaminotriazines |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE474364A (en) |
CH (1) | CH267687A (en) |
GB (1) | GB639218A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3101335A (en) * | 1960-03-01 | 1963-08-20 | Pennsalt Chemicals Corp | Diureidotriazines and process for making |
-
1947
- 1947-07-07 BE BE474364A patent/BE474364A/en unknown
- 1947-07-09 CH CH267687D patent/CH267687A/en unknown
- 1947-07-16 GB GB18996/47A patent/GB639218A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3101335A (en) * | 1960-03-01 | 1963-08-20 | Pennsalt Chemicals Corp | Diureidotriazines and process for making |
Also Published As
Publication number | Publication date |
---|---|
CH267687A (en) | 1950-04-15 |
BE474364A (en) | 1947-08-30 |
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