The multicomponent condensation of an aryl aldehyde, acetyl chloride, acetonitrile, and enolizable ketone as one-pot synthesis of beta-acetamido ketones in high yields was investigated using commercial, non-corrosive, and environmentally benign Keggin and Wells-Dawson heteropolyacid catalysts. The best catalyst was H5PW10V2O40. The methodology used simple experimental conditions, and the short reaction times and high yields indicate it is a useful strategy for the large scale synthesis of beta-acetamido ketones.
机构:
Institut de chimie moléculaire et biologique, L'Ecole Polytechnique Fédérale de Lausanne, Lausanne, SwitzerlandInstitut de chimie moléculaire et biologique, L'Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland
Huang, Xiaogen
Vogel, Pierre
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Institut de chimie moléculaire et biologique, L'Ecole Polytechnique Fédérale de Lausanne, Lausanne, SwitzerlandInstitut de chimie moléculaire et biologique, L'Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland