Reductive bromination of N, N-bis(4-tert-butylphenyl)hydroxylamine


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Resumo

Unlike most arenes, N, N-bis(4-tert-butylphenyl)hydroxylamine reacts with Br2via the reductive bromination mechanism. Here, two hydrogens in ortho positions of benzene rings are substituted by Br2 and provide two-electron reduction of hydroxylamine to amine.

Sobre autores

V. Golubev

Institute of Problems of Chemical Physics, Russian Academy of Sciences

Autor responsável pela correspondência
Email: vgolubev@icp.ac.ru
Rússia, 1 prosp. Akad. Semenova, Chernogolovka, Moscow Region, 142432

Yu. Kim

M. V. Lomonosov Moscow State University

Email: vgolubev@icp.ac.ru
Rússia, 1 Leninskie Gory, Moscow, 119991

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