A convenient method for synthesis of enantiomerically enriched methylphenidate from N-methoxycarbonylpiperidine

Org Lett. 1999 Jul 29;1(2):175-8. doi: 10.1021/ol9905046.

Abstract

[formula: see text] This report describes a new method to prepare optically active methylphenidate starting from piperidine. The method consists of a transformation of N-methoxycarbonylpiperidine to the corresponding alpha-methoxylated carbamate I by utilizing electrochemical oxidation followed by the coupling reaction with optically active Evans imides II to produce optically active methylphenidate derivatives III with high stereoselectivities, threo-(2R,2'R)-Methylphenidate (IV; Ar = Ph; Ritalin) was easily prepared from III in three steps.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic Agents / chemical synthesis*
  • Chromatography, High Pressure Liquid
  • Methylphenidate / chemical synthesis*
  • Piperidines / chemistry
  • Stereoisomerism

Substances

  • Adrenergic Agents
  • N-methoxycarbonylpiperidine
  • Piperidines
  • Methylphenidate