Synfacts 2006(7): 0718-0718  
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

Contributor(s): Paul Knochel, Andrei Gavryushin
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.