反应 #434973
ord-5e3de05ac28342f89a8a676049726120
反应方程式
1-(4-fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-(4-hydroxyphenyl)azetidin-2-one
1-(4-fluorofluorophenyl)-3-[3-(4-fluorofluorophenyl)-3-hydroxypropyl]-4-[4-(2-fluoromethoxyethoxy)phenyl]azetidin-2-one
potassium carbonate
butanesultone
→
product
4-(4-{1-(4-Fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]4-oxoazetidin-2-yl}phenoxy)butane-1-sulfonic acid
反应物
试剂
无
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1过滤The reaction solution was filtered
- 2浓缩concentrated under oil pump vacuum
- 3其他The residue was chromatographed on a 10 g SiO2 cartridge (dichloromethane/methanol=5/1)
- 4其他crystallized from diethyl ether
实验过程
250 mg of 1-(4-fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-(4-hydroxyphenyl)azetidin-2-one (7) were dissolved in 6 ml of absolute dimethylformamide. 337 mg of powdered potassium carbonate and 69 μl of 1,4,-butanesultone were added. The mixture was stirred at room temperature overnight. The reaction solution was filtered and concentrated under oil pump vacuum. The residue was chromatographed on a 10 g SiO2 cartridge (dichloromethane/methanol=5/1) and crystallized from diethyl ether. The product (131 mg) was obtained as a solid.