The Conversion of Amides to Esters with Meerwein'S Reagent. Application to the Synthesis of a Carfentanil Precursor.

AJ Kiessling, CK McClure

Index: Kiessling, Anthony J.; McClure, Cynthia K. Synthetic Communications, 1997 , vol. 27, # 5 p. 923 - 937

Full Text: HTML

Citation Number: 24

Abstract

Abstract An efficient two step transformation of 1° and 2° amides to methyl and ethyl esters has been developed using trimethyl-and triethyloxonium tetrafluoroborates, and dilute acid. This methodology was applied to 1-benzyl-4-phenylamino-4-piperidinecarboxamide, a precursor in the synthesis of carfentanil, to produce the methyl ester in 60% yield and the ethyl ester in 80% yield.