Abstract
Abstract2‐Arylamino‐4,6‐dichloro‐s‐triazine reacts with cyanuric chloride in the presence of alkali to yield N,N‐bis(4,6‐dichloro‐s‐triazin‐2‐yl)‐arylamine. In like manner, 2‐substituted o‐chloro‐, p‐chloro‐, o‐nitro‐ and p‐carbomethoxyphenylamino‐4,6‐dimethoxy‐s‐triazines react with cyanuric chloride to yield the corresponding 4,6‐dichloro‐s‐triazin‐2‐yl‐4′,6′‐dimethoxy‐s‐triazin‐2′‐ylaryl‐amine, while anilino‐, p‐toluidino, o‐ and p‐methoxyphenylamino and o‐carbomethoxyphenylamino derivatives did not.The reaction of cyanuric chloride with 2,4‐dichloro‐6‐ethylamino‐s‐triazine in the presence of alkali yields the condensation product of the ditriazinylamine type and the reaction of cyanuric chloride with ammonia yields N,N‐bis(4,6‐dichloro‐s‐triazin‐2‐yl)‐ or tris(4,6‐dichloro‐s‐triazin‐2‐yl)amine.
Published Version
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