反応 #1528403

ord-73fb2390e4c742809d25e66043eac5a8

反応方程式

Cc1cc(C)c(C(O)c2ccc(C)c(F)c2)c(OCc2ccccc2)n1
2-benzyloxy-4,6-dimethylpyridin-3-yl 3-fluoro-4-methylphenyl methanol
Cc1cc(C)c(Cc2ccc(C)c(F)c2)c(=O)[nH]1
title compound
収率 80.8%
Cc1cc(C)c(Cc2ccc(C)c(F)c2)c(=O)[nH]1
3-(3-Fluoro-4-methylbenzyl)-4,6-dimethyl-1H-pyridin-2-one
収率 80.8%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他After the insoluble material was removed by filtration
  2. 2
    その他the solvent of the filtrate was removed

実験手順

To a solution of 2-benzyloxy-4,6-dimethylpyridin-3-yl 3-fluoro-4-methylphenyl methanol (0.39 g) in ethanol (10 mL) was added a catalytic amount of palladium carbon powder, and the mixture was stirred at room temperature under a hydrogen atmosphere overnight. After the insoluble material was removed by filtration, the solvent of the filtrate was removed to give the title compound (0.22 g).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07655633B2uspto-grants-2010_02