HRID1785265

反应详情

EQUATION

反应方程式

HRID 1785265 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

162 Milligrams of t-butyl 4-((2R)-2-((1R)-3,3-difluorocyclo-pentyl)-2-hydroxy-2-phenylethanoyloxy)tetrahydropyridine-1(2H)-carboxylate was dissolved in 5 ml of 10% hydrochloric acid-methanol, stirred for 12 hours, and the solvent was distilled off under reduced pressure. The residue was diluted with water, washed with diethyl ether and a saturated aqueous sodium hydrogencarbonate solution was added to the aqueous layer to render it alkaline. Following an extraction with ethyl acetate, the organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. Distilling the solvent off under reduced pressure, 104 mg of the title compound was obtained as a colorless, foamy substance.

WORKUP

后处理

  1. distillationthe solvent was distilled off under reduced pressure
  2. additionThe residue was diluted with water
  3. washwashed with diethyl ether
  4. additiona saturated aqueous sodium hydrogencarbonate solution was added to the aqueous layer
  5. extractionan extraction with ethyl acetate
  6. washthe organic layer was washed with saturated brine
  7. dry with materialdried over anhydrous sodium sulfate
  8. distillationDistilling the solvent off under reduced pressure