Anodic oxidation of 2- and 4'-substituted benzenesulfenanilides. A new method of synthesis of 2,7-disubstituted phenazines.

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Anodic oxidations of benzenesulfenanilides (4'-OMe (I), 4'-Me (II), 4'-Cl (III), 4'-H (IV) ) and 2-nitrobenzenesulfenanilides (4'-OMe (V), 4'-Me (VI), 4'-Cl (VII), 4'-H (VIII) ) were carried out in acetonitrile containing 0.1 M NaClO4. electrolyses of I, II, V, VI, and VII gave the corresponding 2, 7-disubstituted phenazines, whereas those of III, IV, and VIII did not. The R-N. intermediates are suggested for the formation of the phenazines.

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