Triazine isocyanates: Part II: Reaction of 2,4-diamino-s-triazines with ethyl chlorocarbonate
โ Scribed by E. F. J. Duynstee; Th. Veerkamp
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 504 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0165-0513
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โฆ Synopsis
Abstract
Benzoguanamine (2,4โdiaminoโ6โphenylโsโtriazine) and acetoguanamine (2,4โdiaminoโ6โmethylโsโtriazine) both react with an excess of ethyl chlorocarbonate; in this reaction two hydrogen atoms from the guanamines are replaced by two carbethoxy groups. The I.R. spectrum reveals that this double substitution takes place on one amino group; in consequence, the resulting compounds are derivatives of iminodicarboxylic acid diethyl ester. Upon heating above the melting point, the compounds decompose, during which process a very short occurrence of isocyanate absorption can be observed in the I.R. spectrum.
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