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Triazine isocyanates: Part II: Reaction of 2,4-diamino-s-triazines with ethyl chlorocarbonate

โœ 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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โœฆ Synopsis


Abstract

Benzoguanamine (2,4โ€diaminoโ€6โ€phenylโ€sโ€triazine) and acetoguanamine (2,4โ€diaminoโ€6โ€methylโ€sโ€triazine) 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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