反应 #6334
ord-4f75d89850dd4de3a07f2755539ba444
反应方程式
3
4-(2-carbethoxy-1-ethyl)-7-methoxy-2-oxo-2H-1-Benzopyran
AlCl3
EtSH
→
4
收率 27.1%
4-(2-carbethoxy-1-ethyl)-7-hydroxy-2-oxo-2H-1-Benzopyran
收率 27.1%
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1其他The ice bath was removed
- 2其他The solvents were removed in vacuo
- 3其他the residue thoroughly vacuum dried
- 4萃取The residue was extracted into EtOAc as much as possible, then the extract
- 5其他chromatographed
实验过程
To a suspension of 726 mg (5.4 mmol) of AlCl3 in 10 mL of dichloromethane at 0° C. was added 4 mL of EtSH. The suspension became a clear solution within seconds. Then, 298 mg (1.08 mmol) of 3 in 4 mL of dichloromethane was added, turning the yellow solution red in color. The ice bath was removed, and the reaction stirred to room temperature for 3 h. The solvents were removed in vacuo, and the residue thoroughly vacuum dried. The residue was extracted into EtOAc as much as possible, then the extract was flash chromatographed using 30/70 EtOAc/hexane. The long- and short-wave UV active band gave 76.7 mg (27%) of 4.