HRID579388

反应详情

EQUATION

反应方程式

HRID 579388 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Ethyl 2-{4-[(9R)-9-hydroxy-2-(3-hydroxy-3-methylbutyloxy)-9-(trifluoromethyl)-9H-fluoren-4-yl]-1H-pyrazol-1-yl}-2-methylpropionate (68.4 g) was dissolved in ethanol (256 ml), 4N aqueous sodium hydroxide (128 ml) was added, and the mixture was stirred at room temperature for 2.5 hr. The reaction mixture was ice-cooled, 2N hydrochloric acid (333 ml) was added dropwise, and the mixture was extracted with ethyl acetate (500 ml). The obtained organic layer was washed successively with water (400 ml, twice) and saturated brine (400 ml). The obtained organic layer was dried over anhydrous sodium sulfate, the insoluble material was filtered off, and the solvent in the filtrate was evaporated to give the title compound (70.0 g).

WORKUP

后处理

  1. temperaturecooled
  2. extractionthe mixture was extracted with ethyl acetate (500 ml)
  3. washThe obtained organic layer was washed successively with water (400 ml
  4. dry with materialThe obtained organic layer was dried over anhydrous sodium sulfate
  5. filtrationthe insoluble material was filtered off
  6. customthe solvent in the filtrate was evaporated