HRID1247381

反应详情

EQUATION

反应方程式

HRID 1247381 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
65 °C

PROCEDURE

实验过程

To a solution of (RS)-[3-(tert-butyl-diphenyl-silanyloxy)-2,6-difluoro-phenyl]-ethoxy-acetic acid ethyl ester (62.5 g) in THF (250 ml) and MeOH (250 ml) was added H2O (200 ml) and LiOH.H2O (10.5 g) and it was stirred 2 h at 65° C. MeOH and THF were evaporated and the aqueous residue was washed with Hept/Et2O 9:1 (2×150 ml). The organic layers were extracted with two portions of H2O (200 ml). The combined aqueous layers were cooled in an ice bath and acidified with 35 ml 25% aq. HCl. Extraction with AcOEt (3×200 ml) followed by washing with brine, drying (Na2SO4) and evaporation of the solvent afforded 28.7 g (99%) of (RS)-(2,6-difluoro-3-hydroxy-phenyl)-ethoxy-acetic acid. Yellow viscous oil. MS 231.2 ([M−H]−).

WORKUP

后处理

  1. customMeOH and THF were evaporated
  2. washthe aqueous residue was washed with Hept/Et2O 9:1 (2×150 ml)
  3. extractionThe organic layers were extracted with two portions of H2O (200 ml)
  4. temperatureThe combined aqueous layers were cooled in an ice bath
  5. extractionExtraction with AcOEt (3×200 ml)
  6. washby washing with brine
  7. customdrying
  8. custom(Na2SO4) and evaporation of the solvent