Issue 4, 1985

The synthesis of diarylamines by nitro-group displacement. Activation of anilines containing electron-withdrawing groups by potassium carbonate

Abstract

Anilines of enhanced N-acidity can displace activated aromatic nitro-groups in dipolar aprotic solvents in the presence of potassium carbonate; the resulting diarylamines are generally obtained free of triarylamine and of the hydrogen displacement product.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 238-239

The synthesis of diarylamines by nitro-group displacement. Activation of anilines containing electron-withdrawing groups by potassium carbonate

J. H. Gorvin, J. Chem. Soc., Chem. Commun., 1985, 238 DOI: 10.1039/C39850000238

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