反应 #1552029

反应方程式

ammonium chloride

4-(3-propylcyclopentyl)-cyclohexanone

1-bromo-4-ethoxy-2,3-difluorobenzene

n-Butyllithium

→

1-(4-ethoxy-2,3-difluorophenyl)-4-(3-propylcyclopentyl)cyclohexanol

收率 94.7%

溶剂

THF

THF

hexane

反应条件

后处理

1. 1
   温度it was warmed to room temperature
2. 2
   其他The mixture was separated
3. 3
   萃取the water layer was extracted with ethyl acetate three times
4. 4
   洗涤the combined organic layer was washed with brine
5. 5
   干燥The solution was dried over anhydrous magnesium sulfate
6. 6
   workup.DISTILLATIONthe solvent was distilled off under reduced pressure
7. 7
   其他The residue was purified by silica gel chromatography (eluent: ethyl acetate/n-heptane=1/9 by volume)

实验过程

THF (100 ml) was added to 1-bromo-4-ethoxy-2,3-difluorobenzene (5.1 g) in a reaction vessel under an atmosphere of nitrogen, and the mixture was cooled to −78° C. n-Butyllithium (1.57 M, in a hexane solution) (13.8 ml) was added dropwise at a temperature of −70° C. or lower. The stirring was continued at −78° C. for another 2 hours, and 4-(3-propylcyclopentyl)-cyclohexanone (3.0 g) in a THF (10 ml) solution was added dropwise at a temperature of −70° C. or lower. After the mixture had been stirred at −78° C. for another 1 hour, it was warmed to room temperature, and a saturated aqueous solution of ammonium chloride (50 ml) was added. The mixture was separated, and the water layer was extracted with ethyl acetate three times, and then the combined organic layer was washed with brine. The solution was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (eluent: ethyl acetate/n-heptane=1/9 by volume) to give 1-(4-ethoxy-2,3-difluorophenyl)-4-(3-propylcyclopentyl)cyclohexanol (5.0 g).

来源