Skip to Content
Merck
CN
  • Preparation of hydantoins by catalytic oxidative carbonylation of alpha-amino amides.

Preparation of hydantoins by catalytic oxidative carbonylation of alpha-amino amides.

The Journal of organic chemistry (2009-10-30)
Seth M Dumbris, Delmy J Díaz, Lisa McElwee-White
ABSTRACT

Hydantoins can be synthesized from the corresponding amino amides employing oxidative catalytic carbonylation using W(CO)(6) as the catalyst, I(2) as the oxidant, CO as the carbonyl source, and DBU as base. Secondary amides afford the hydantoins in good to excellent yields, which decrease as the steric bulk of the N-alkyl substituent increases.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Tungsten hexacarbonyl, packaged for use in deposition systems
Sigma-Aldrich
Tungsten hexacarbonyl, 99.99% trace metals basis (excluding Mo), purified by sublimation
Sigma-Aldrich
Tungsten hexacarbonyl, 97%