PECULIARITIES OF OXYCHLORINATION AND OXYBROMINATION REACTIONS OF AROMATIC AMINES
Oxyhalogenation reaction of aniline with electron-donor and electron-acceptor subsituents in o-, m-, p- positions of aromatic ring has been investigated, the peculiarities of oxychlorination and oxybromination reaction depending on conditions have been determined, the compositions and structures of the prepared products have been studied.
Keywords : oxyhalogenation, o-, m-, p-substituted anilines, spatial hindrance, “ortho-effect”, brominated tolyidines and anizidines
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