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The Gomberg-Bachmann reaction for the arylation of anilines with aryl diazotates.

Chemistry (Weinheim an der Bergstrasse, Germany) (2012-08-14)
Gerald Pratsch, Tina Wallaschkowski, Markus R Heinrich
ABSTRAKT

Simply aqueous sodium hydroxide is sufficient to exclude ionic side reactions and to prepare 2-aminobiphenyls from aryl diazotates and anilines through a new variant of the Gomberg-Bachmann reaction (see scheme). The metal-free reaction under basic conditions allows to exploit the highly radical-stabilizing effect of the aniline's free amino function for the first time, which leads to a so far unreached regioselectivity.

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Sigma-Aldrich
2-Aminobiphenyl, ≥96.5% (GC)