反应 #2175425

反应方程式

ammonia

Lithium aluminum hydride

trans-4-(4-Hexyloxy-2,3-difluorophenyl)-cyclohexanecarboaldehyde

ethyl acetate

→

trans-4-(4-hexyloxy-2,3-difluorophenyl)-hydroxymethylcyclohexane

收率 29.6%

溶剂

THF

反应条件

后处理

1. 1
   温度cooling
2. 2
   其他deposits were removed by filtration through Celite
3. 3
   萃取The filtrate was extracted with ethyl acetate
4. 4
   洗涤The combined organic phase was washed successively with water and brine
5. 5
   干燥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 recrystallization from heptane

实验过程

Lithium aluminum hydride (1.1 g) was suspended in THF (200 ml). trans-4-(4-Hexyloxy-2,3-difluorophenyl)-cyclohexanecarboaldehyde (s-15) (15.8 g) was added dropwise to the suspension in the temperature range of −20° C. to −10° C., and the stirring was continued in this temperature range for 2 hours. After the completion of the reaction had been confirmed by means of GC analysis, ethyl acetate and then a saturated aqueous solution of ammonia were added to the reaction mixture under ice-cooling and deposits were removed by filtration through Celite. The filtrate was extracted with ethyl acetate. The combined organic phase was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was purified by recrystallization from heptane to give trans-4-(4-hexyloxy-2,3-difluorophenyl)-hydroxymethylcyclohexane (s-16) (4.7 g). The yield based on the compound (s-15) was 29.6%.

来源