反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 80 °C
PROCEDURE
实验过程
To an oven-dried three-neck round-bottom flask under nitrogen, were added 25.97 g of 2,7-dibromofluorene, 32.06 g sodium hydroxide, 1.33 g KI, and 300 mL anhydrous DMSO. The 46 g 3-(4-bromobutyl)bicyclo[4.2.0]octa-1(6),2,4-triene 300 mL anhydrous DMSO was added via cannula. The reaction was heated to 80° C. After 4 hours, the reaction was quenched by the addition of DI water (10 mL). The excess salt was removed by filtration. 500 mL Ethyl acetate was added, and extracted with DI water (3×300 mL) and brine (3×300 mL). The combined organic layer was dried over anhydrous magnesium sulfate. Magnesium sulfate was removed by filtration, and the solvent was removed by rotary evaporation. The product (43 g) was purified by flash chromatography using hexane. The structure was confirmed by NMR.
WORKUP
后处理
- customthe reaction was quenched by the addition of DI water (10 mL)
- customThe excess salt was removed by filtration
- addition500 mL Ethyl acetate was added
- extractionextracted with DI water (3×300 mL) and brine (3×300 mL)
- dry with materialThe combined organic layer was dried over anhydrous magnesium sulfate
- customMagnesium sulfate was removed by filtration
- customthe solvent was removed by rotary evaporation
- customThe product (43 g) was purified by flash chromatography