HRID971271

反应详情

EQUATION

反应方程式

HRID 971271 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

A solution of 4-(3-fluoro-phenyl)-4-oxo-butyric acid methyl ester (28.27 g, 134.49 mmol), hydrazine monohydrate (26.1 mL, 26.93 g, 537.96 mmol) and KOH (22.64 g, 403.47 mmol) in ethylene glycol (150 mL) was heated to reflux under argon and refluxed for 2 hours. The reaction mixture was cooled and diluted with 1.5 litres of water, 500 mL of Et2O was added, and the mixtures was acidified by addition of 6 M HCl with stirring, after which an additional 500 mL of Et2O was added. The organic layer was removed and the aqueous layer was extracted twice with 250 mL of 500 mL of Et2O/EtOAc (3:1). The combined organic layers were washed with water, saturated brine, and then dried over MgSO4. The solvent was evaporated under reduced pressure to yield a brownish oil, which was eluted through silica gel using hexanes/EtOAc (9:1). Removal of solvent under reduced pressure yielded 18.44 g (101.21 mmol, 75.26%) of 4-(3-fluoro-phenyl)-butyric acid as an oil. MS: 183 (M+H)+.

WORKUP

后处理

  1. temperatureto reflux under argon
  2. temperaturerefluxed for 2 hours
  3. temperatureThe reaction mixture was cooled
  4. additionwas added
  5. customThe organic layer was removed
  6. extractionthe aqueous layer was extracted twice with 250 mL of 500 mL of Et2O/EtOAc (3:1)
  7. washThe combined organic layers were washed with water, saturated brine
  8. dry with materialdried over MgSO4
  9. customThe solvent was evaporated under reduced pressure
  10. customto yield a brownish oil, which
  11. washwas eluted through silica gel
  12. customRemoval of solvent under reduced pressure