HRID2202661

反应详情

EQUATION

反应方程式

HRID 2202661 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

n-BuLi (2.6 M in hexane, 2.3 mL, 5.94 mmol) was added dropwisely to a stirred solution of (methoxymethyl)triphenylphosphonium chloride (2.04 g, 5.94 mmol) in THF (20 mL) at −78° C. and stirred for 10 min at the same temperature and then stirred for 2.5 h at room temperature. The reaction mixture was cooled down to −78° C., a solution of 4,4-dimethylcyclohexanone (500 mg, 3.96 mmol) in THF (5 mL) was added slowly at −78° C. The reaction mixture was allowed to warm to room temperature and stirred at room temperature for overnight. The reaction mixture was quenched with sat. NaHCO3 aq. (20 mL) and extracted with EtOAc. The combined organic layers were dried over anhydrous Na2SO4 and concentrated under reduced pressure to provide compound A12-1 (512.2 mg, crude) as pale yellow oil. The crude product was used for next step without purification.

WORKUP

后处理

  1. stirringstirred for 2.5 h at room temperature
  2. temperatureto warm to room temperature
  3. stirringstirred at room temperature for overnight
  4. customThe reaction mixture was quenched with sat. NaHCO3 aq. (20 mL)
  5. extractionextracted with EtOAc
  6. dry with materialThe combined organic layers were dried over anhydrous Na2SO4
  7. concentrationconcentrated under reduced pressure
  8. customto provide compound A12-1 (512.2 mg, crude) as pale yellow oil
  9. customThe crude product was used for next step without purification