106. p-Aminodimethylaniline. Part III. The orientation of groups in the disubstituted molecule

EE Ayling, JH Gorvin, LE Hinkel

Index: Ayling; Gorvin; Hinkel Journal of the Chemical Society, 1946 , p. 530

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Citation Number: 1

Abstract

The study of the influence of nuclear substituents on the coupling power of diazotised p- aminodimethylaniline (compare Parts I and 11, J., 1941, 613; 1942, 755) required the preparation of derivatives of the base having chloro-or nitro-groups in the o-and m-positions to the dimethylamino-group. 2-Chloro-4-acetamidodimethylaniline yields the 6-nitro- derivative by nitration in sulphuric acid. In the chlorination of $-nitro-4- ...