Chem. J. Chinese Universities ›› 2000, Vol. 21 ›› Issue (S1): 465.

• Synthetic Sciences • Previous Articles     Next Articles

A Convenient Method for Synthesis Methyl Ester of Naproxen

LI Yan-Yun, XIA Chun-Gu   

  1. State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000
  • Online:2000-12-31 Published:2000-12-31

Abstract:

α-Arylpropionic acids are a class of nonsteroidal anti-inflammatory drugs with a substantial size of market. Ibuprofen and naproxen are the important members of this family. Since carbonylation catalyzed by transition metal complexes provides an environmentally benign process for their synthesis, there have been numerous patents and publications related to the carbonylation of alcohols and olefins to produce α-arylpropionic acids or their esters[1-4]. We have studied the carbonylation of α-(6'-methoxy-2'-naphthyl) ethanol to methyl ester of naproxen using PVP-PdCl2-CuCl2/PPh3 catalyst system. Good conversion and selectivity were obtained under mild conditions.

TrendMD: