HRID237717

反应详情

EQUATION

反应方程式

HRID 237717 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
50 °C

PROCEDURE

实验过程

1 M aqueous NaOH solution (310 μL) is added to a solution of methyl 2-((S)-6-((R)-7-fluoro-4-(4-(3-hydroxy-3-methylbutyl)-2,6-dimethylphenyl)-2,3-dihydro-1H-inden-1-yloxy)-2,3-dihydrobenzofuran-3-yl)acetate (110 mg) in methanol (4 mL). The mixture is stirred at room temperature for 12 hours and at 50° C. for 2 days. 1 M aqueous NaOH solution (100 μL) is added and the mixture is stirred at 50° C. for 1 hour. Methanol is evaporated in vacuo, the residue is diluted with water and neutralized with 1 M aqueous HCl. The resulting mixture is extracted with ethyl acetate, and the combined organic phases are washed with brine and dried (MgSO4). The solvent is evaporated to give the title compound. Yield: 80 mg; LC (method 8): tR=0.59 min; Mass spectrum (ESI+): m/z=519 [M+H]+.

WORKUP

后处理

  1. stirringthe mixture is stirred at 50° C. for 1 hour
  2. customMethanol is evaporated in vacuo
  3. additionthe residue is diluted with water and neutralized with 1 M aqueous HCl
  4. extractionThe resulting mixture is extracted with ethyl acetate
  5. washthe combined organic phases are washed with brine
  6. dry with materialdried (MgSO4)
  7. customThe solvent is evaporated