HRID404329

反应详情

EQUATION

反应方程式

HRID 404329 的结构方程式

CONDITIONS

反应条件

温度
23 °C

PROCEDURE

实验过程

To a stirred solution of 2′-fluoro-5′-(methyloxy)-2-((methyloxy)carbonyl)-1,1′-biphenyl-4-carboxylic acid T4.3 (35.60 g, 117 mmol) in THF (1170 mL, 117 mmol) at 0° C. was added borane-THF (234 mL, 234 mmol). The reaction was warmed to 23° C., and the mixture was stirred for 6 hours. The mixture was then concentrated in vacuo. 1 N HCl was added, and the mixture was extracted with EtOAc. The organic layers were combined, dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified on silica gel (0-40% EtOAc in hexane) to give methyl 2′-fluoro-4-(hydroxymethyl)-5′-(methyloxy)-1,1′-biphenyl-2-carboxylate T4.4 as a clear oil (30.00 g, 88% yield). MS ESI (pos.) m/e: 308.0 (M+H2O)+, 291.1 (M+H)+.

WORKUP

后处理

  1. concentrationThe mixture was then concentrated in vacuo
  2. addition1 N HCl was added
  3. extractionthe mixture was extracted with EtOAc
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified on silica gel (0-40% EtOAc in hexane)