Reacción #1528403

ord-73fb2390e4c742809d25e66043eac5a8

Ecuación de reacción

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
Rendimiento 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
Rendimiento 80.8%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroAfter the insoluble material was removed by filtration
  2. 2
    Otrothe solvent of the filtrate was removed

Procedimiento

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).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07655633B2uspto-grants-2010_02