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NIS-catalyzed reactions: amidation of acetophenones and oxidative amination of propiophenones.

Chemistry (Weinheim an der Bergstrasse, Germany) (2012-10-09)
Manjunath Lamani, Kandikere Ramaiah Prabhu
ZUSAMMENFASSUNG

Single-step amination: the N-iodosuccinimide (NIS)-catalyzed amidation of acetophenone derivatives by using tert-butylhydroperoxide (TBHP) as an oxidant is presented. A variety of acetyl derivatives of heterocyclic compounds were easily converted to their corresponding ketoamides under these conditions. A new, NIS-catalyzed amination of propiophenone and its derivatives in the presence of TBHP to furnish the corresponding 2-aminoketone derivatives is the first reported single-step amination of propiophenone derivatives.

MATERIALIEN
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Marke
Produktbeschreibung

Sigma-Aldrich
N-Iodsuccinimid, 95%