HRID244961

反应详情

EQUATION

反应方程式

HRID 244961 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To 60 mL of tetrahydrofuran and 9.3 mL (66 mmol) of diisopropylamine, 38 mL (60 mmol) of 1.57 M n-butyllithium in n-hexane was added dropwise under a nitrogen atmosphere under cooling with ice, and the reaction mixture was warmed to room temperature and stirred for 30 minutes. After the stirring, the reaction mixture was cooled to −78° C., and after dropwise addition of 4.62 g (30.0 mmol) of ethyl 2-(furan-2-yl)acetate, stirred at the same temperature for 1 hour. After the stirring, 3.8 mL (36 mmol) of isobutyryl chloride was added at −78° C., and the reaction mixture was gradually warmed and then stirred at room temperature for 15 hours. After completion of the reaction, the reaction mixture was diluted with saturated aqueous ammonium chloride under cooling with ice and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate and with saturated aqueous sodium chloride successively, dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by intermediate pressure silica gel column chromatography (silica gel 30 g, ethyl acetate:hexane=1:10) to give 22 g of the desired product as an orange liquid.

WORKUP

后处理

  1. temperatureunder cooling with ice
  2. temperatureAfter the stirring, the reaction mixture was cooled to −78° C.
  3. stirringstirred at the same temperature for 1 hour
  4. temperaturethe reaction mixture was gradually warmed
  5. stirringstirred at room temperature for 15 hours
  6. customAfter completion of the reaction
  7. temperatureunder cooling with ice
  8. extractionextracted with ethyl acetate
  9. washThe organic layer was washed with saturated aqueous sodium hydrogen carbonate and with saturated aqueous sodium chloride successively
  10. dry with materialdried over anhydrous magnesium sulfate
  11. filtrationfiltered
  12. concentrationthe filtrate was concentrated under reduced pressure
  13. customThe resulting residue was purified by intermediate pressure silica gel column chromatography (silica gel 30 g, ethyl acetate:hexane=1:10)