反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Stir 1-(3-bromo-2-hydroxy-4-methoxy-phenyl)-ethanone (20 g, 82 mmol) in dichloromethane (500 mL) at −30° C. under a nitrogen atmosphere. Treat with boron tribromide (30 mL, 318 mmol) and stir over night at room temperature. Pour mixture into cracked ice and stir for 1 hr. Extract twice with dichloromethane, wash organic layers with water, saturated aqueous sodium chloride solution, dry with magnesium sulfate, filter, and evaporate filtrate. Chromatograph residue on silica gel eluting with 2:1 dichloromethane/hexane to provide the title compound (13.8 g, 74% yield) as an off white powder. 1H NMR (CDCl3) δ 13.5 (s, 1H), 7.65 (d, J=8.0 Hz, 1H), 6.62 (d, J=8.0 Hz, 1H), 6.20 (s, 1H), 2.60 (s, 3H).
Pour mixture into cracked ice
stir for 1 hr
Extract twice with dichloromethane
wash organic layers with water, saturated aqueous sodium chloride solution
dry with magnesium sulfate
filter
evaporate filtrate
来源 ID: ord-0306c0c9a52e4fbbaaec6dd702f03d05