反应 #1256743
ord-b92f8a893a6b4bbb9a3f7e70a4b33521
反应方程式
反应物
试剂
反应条件
后处理
- 1workup.WAITThe reaction mixture was left
- 2温度to cool
- 3洗涤The formed organic layer was washed three times with water
- 4干燥by drying over sodium sulfate anhydrate
- 5其他The solvent was removed
- 6workup.DISTILLATIONfollowed by purification through distillation under reduced pressure, whereby the Compound 40a
- 7其他was obtained as a colorless liquid (boiling point; 70 mmHg, 102 to 106° C. fraction, 8.26 g, 50%)
实验过程
Diisopropylchlorosilane (16.4 mL, 96.1 mmol) was dissolved in THF (100 mL), and isobutylmagnesium bromide THF solution (1.0M, 100 mL) was added dropwise thereto under nitrogen for 30 minutes. Subsequently, cuprous bromide (286 mg, 2.00 mmol) was added to the resultant mixture, followed by stirring at 70° C. overnight. The reaction mixture was left to cool, and saturated aqueous ammonium chloride and n-pentane were added thereto. The formed organic layer was washed three times with water and once with saturated brine, followed by drying over sodium sulfate anhydrate. The solvent was removed, followed by purification through distillation under reduced pressure, whereby the Compound 40a was obtained as a colorless liquid (boiling point; 70 mmHg, 102 to 106° C. fraction, 8.26 g, 50%).