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Synfacts 2006(7): 0718-0718
DOI: 10.1055/s-2006-941885
DOI: 10.1055/s-2006-941885
Metal-Mediated Synthesis
© Georg Thieme Verlag Stuttgart · New York
Pd(0)-Catalyzed Reduction of Aromatic Acid Chlorides to Aldehydes
K. Lee, Jr. R. E. Maleczka*
Michigan State University, East Lansing, USA
Further Information
Publication History
Publication Date:
22 June 2006 (online)

Significance
This method is a further development of a previously published protocol of the acid chloride reduction in the presence of an organotin catalyst. Importantly, the authors have proven that a silane itself can be used as a reducing agent, thus avoiding the use of toxic tin compounds. The reaction proceeds at ambient temperature within an hour, and the yields are uniformly good. A halide substituent on the aryl ring remains intact during the reaction.