HRID383482

反应详情

EQUATION

反应方程式

HRID 383482 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

To a −78° C. stirred solution of 4-hydroxy-5,5-dimethyl-5H-furan-2-one (250 mg, 1.95 mmol) in 18 mL of anhydrous CH2Cl2, was added triethylamine (0.40 mL, 2.9 mmol) and Tf2O (0.49 mL, 2.9 mmol). The reaction was stirred at −78° C. for 30 minutes, and quenched with saturated NH4Cl solution (10 mL). The mixture was warmed up to room temperature and separated. The aqueous layer was extracted with CH2Cl2 (2×20 mL). All organic layers were combined, dried over Na2SO4 and evaporated to brown oil, which was purified by plugging through a short pad of silica gel column with EtOAc/hexanes (1/3). Evaporation of solvents gave 2,2-dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonate as a light brown oil (450 mg, 89%).

WORKUP

后处理

  1. customquenched with saturated NH4Cl solution (10 mL)
  2. temperatureThe mixture was warmed up to room temperature
  3. customseparated
  4. extractionThe aqueous layer was extracted with CH2Cl2 (2×20 mL)
  5. dry with materialdried over Na2SO4
  6. customevaporated to brown oil, which
  7. customwas purified
  8. customEvaporation of solvents