Substituent effects in the bis (benzotriazolylmethylation) of aromatic amines

AR Katritzky, S Rachwal, J Wu

Index: Katritzky, Alan R.; Rachwal, Stanislaw; Wu, Jing Canadian Journal of Chemistry, 1990 ,  vol. 68,  # 3  p. 446 - 455

Full Text: HTML

Citation Number: 32

Abstract

1-(Hydroxymethyl) benzotriazole and aromatic amines react to give an equilibrium mixture of N-mono-and N, N-bis (benzotriazolylmethyl) arylamines. Electron-releasing substituents on the arylamine ring shift the equilibrium towards the N, N-bis (benzotriazolylmethylated) products, and removal of water formed in the reaction leads to these bis derivatives in quantitative yields. These products were isolated as mixtures of three isomers, the ...

Related Articles:

More Articles...