HRID216373

反应详情

EQUATION

反应方程式

HRID 216373 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A solution of ethyl bromo(difluoro)acetate (0.53 mL, 4.1 mmol) and 1-[4-(5-fluoropyridin-2-yl)phenyl]ethanone (800 mg, 3.7 mmol) in tetrahydrofuran (40 mL) was added to a 0.1 M solution of samarium diiodide in tetrahydrofuran (82 mL, 8.2 mmol) at ambient temperature. After stirring at ambient temperature for 3 min, the reaction was cooled and quenched with 1N aqueous hydrochloric acid. Volatiles were removed in vacuo and the residue was partitioned between ethyl acetate and 1 N hydrochloric acid. The organic phase was washed with saturated aqueous sodium bicarbonate and brine, dried (sodium sulfate) and concentrated in vacuo. Chromatography over silica eluting with 0-40% ethyl acetate/hexane afforded ethyl 2,2-difluoro-3-[4-(5-fluoropyridin-2-yl)phenyl]-3-hydroxybutanoate.

WORKUP

后处理

  1. temperaturethe reaction was cooled
  2. customquenched with 1N aqueous hydrochloric acid
  3. customVolatiles were removed in vacuo
  4. customthe residue was partitioned between ethyl acetate and 1 N hydrochloric acid
  5. washThe organic phase was washed with saturated aqueous sodium bicarbonate and brine
  6. dry with materialdried (sodium sulfate)
  7. concentrationconcentrated in vacuo