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
- -78 °C
PROCEDURE
实验过程
2,6-Dibromo-4,8-dimethoxy-benzo[1,2-b:4,5-b′]dithiophene (500 mg, 1.22 mmol., 1.00 equiv.) and dichloromethane (12 mL) were added to a 50 mL schlenk flask. The mixture was cooled to −78 ° C. and boron tribromide was added (1.0 M solution in dichloromethane, 2.5 mL, 2.5 mmol., 2.1 equiv.) slowly. The mixture was stirred for 15 minutes at −78° C. before replacing the dry/ice acetone bath with an ice/water bath. The reaction mixture was left to warm to room temperature while stirring for 16 hours before cooling to 0° C. Water (dropwise at first, 150 mL total) and additional dichloromethane (50 mL) were added. The dichloromethane was removed on the rotary evaporator and the solid was collected by filtration. The solid was washed with water (25 mL) and dichloromethane (25 ml) to give a pale blue/green crude solid to be dried under vacuum and used in the next step without additional purification (287 mg). 1H NMR (400 MHz, CDCl3) δ 10.13 (s, 2H), 7.71 (s, 2H).
WORKUP
后处理
- customdry/ice acetone bath with an ice/water bath
- waitThe reaction mixture was left
- temperatureto warm to room temperature
- stirringwhile stirring for 16 hours
- temperaturebefore cooling to 0° C
- additionWater (dropwise at first, 150 mL total) and additional dichloromethane (50 mL) were added
- customThe dichloromethane was removed on the rotary evaporator
- filtrationthe solid was collected by filtration
- washThe solid was washed with water (25 mL) and dichloromethane (25 ml)
- customto give a pale blue/green crude solid
- customto be dried under vacuum
- customused in the next step without additional purification (287 mg)