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Aldehydes as Alkylating Agents for Ketones
Authors:Sofiya A. Runikhina  Dr. Oleg I. Afanasyev  Klim Biriukov  Prof. Dr. Dmitry S. Perekalin  Dr. Martin Klussmann  Dr. Denis Chusov
Affiliation:1. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Vavilova St. 28, 119991 Moscow, Russia;2. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Vavilova St. 28, 119991 Moscow, Russia

G.V. Plekhanov Russian University of Economics, 36 Stremyanny Per., 117997 Moscow, Russia;3. Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr, Germany

Abstract:Common and non-toxic aldehydes are proposed as reagents for alkylation of ketones instead of carcinogenic alkyl halides. The developed reductive alkylation reaction proceeds in the presence of the commercially available ruthenium catalyst [(cymene)RuCl2]2 (as low as 250 ppm) and carbon monoxide as the reducing agent. The reaction works well for a broad substrate scope, including aromatic and aliphatic aldehydes and ketones. It can be carried out without a solvent and often gives nearly quantitative yields of the products. This straightforward and cost-effective method is promising not only for laboratory application but also for industry, which produces carbon monoxide as a large-scale waste product.
Keywords:aldehydes  alpha-alkylation  ketones  reductive coupling  ruthenium
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