HRID397162

反应详情

EQUATION

反应方程式

HRID 397162 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

To a stirring solution of 4-fluorophenylmethyl triphenylphosphonium chloride (39 g, 96 mmol, Lancaster) in 500 mL of dry THF at −78° C. was added 1 M potassium t-butoxide in THF (106 mL, 106 mmol, Aldrich). The reaction was stirred for 30 min and then warmed to 0° C. The reaction was stirred for 30 min and then 1,4-cyclohexanedione mono-ethylene ketal (15.0 g, 96 mmol, Aldrich) was added. After 30 min, the reaction was warmed to room temperature and allowed to stir overnight. The reaction was heated to reflux for 4 h and then cooled to room temperature. The reaction was quenched with saturated ammonium chloride (500 mL) and ethyl acetate (500 mL). The organic layer was separated, washed with brine, dried over sodium sulfate, and conc in vacuo to a white solid. The solid was purified by flash chromatography (SiO2, 19:1 hexanes:ethyl acetate) to yield 18.9 g of a colorless oil. MS (ESI) 251 (M+H).

WORKUP

后处理

  1. stirringThe reaction was stirred for 30 min
  2. waitAfter 30 min
  3. temperaturethe reaction was warmed to room temperature
  4. stirringto stir overnight
  5. temperatureThe reaction was heated
  6. temperatureto reflux for 4 h
  7. temperaturecooled to room temperature
  8. customThe reaction was quenched with saturated ammonium chloride (500 mL) and ethyl acetate (500 mL)
  9. customThe organic layer was separated
  10. washwashed with brine
  11. dry with materialdried over sodium sulfate
  12. customThe solid was purified by flash chromatography (SiO2, 19:1 hexanes:ethyl acetate)