反应 #1463485

反应方程式

tetrahydrofuran

tetrahydrofuran

4-(4-propylcyclohexyl)cyclohexanone

potassium t-butoxide

triphenylphosphonium bromide

→

4-(4-propylcyclohexyl)cyclohexane

收率 56.0%

溶剂

ether

反应条件

后处理

1. 1
   其他Into a three-necked flask equipped with a dropping funnel
2. 2
   其他reached 10° C
3. 3
   其他up to room temperature
4. 4
   其他for one hour
5. 5
   workup.STIRRINGstirring for one hour
6. 6
   workup.STIRRINGfurther stirring the reaction mixture for 5 hours
7. 7
   workup.ADDITIONafter completion of the dropwise addition
8. 8
   过滤filtering off
9. 9
   浓缩concentrating the filtrate under reduced pressure
10. 10
    其他isolating
11. 11
    其他purifying the resulting pale brown oily substance by means of silica gel column chromatography
12. 12
    其他recrystallizing from ethanol

实验过程

Into a three-necked flask equipped with a dropping funnel, a three-way cock and a thermometer was placed (2-(1,3-dioxan)-2-yl)ethyl)triphenylphosphonium bromide (12.3 g, 27 mmols), followed by adding tetrahydrofuran (50 ml), suspending, stirring under ice cooling till the liquid temperature reached 10° C. The reaction mixture is added potassium t-butoxide (3.0 g, 27 mmols), followed by elevating the temperature up to room temperature under ice cooling for one hour, stirring for one hour, dropwise adding a tetrahydrofuran (10 ml) solution of 4-(4-propylcyclohexyl)cyclohexanone (15.6 g, 25 mmols) over 30 minutes from the dropping funnel, further stirring the reaction mixture for 5 hours after completion of the dropwise addition, adding ether (50 ml), allowing to stand for one hour, filtering off deposited insoluble substance, concentrating the filtrate under reduced pressure, isolating and purifying the resulting pale brown oily substance by means of silica gel column chromatography and recrystallizing from ethanol, to obtain 1-(2-(1,3-dioxin)-2-yl)ethylidene)-4-(4-propylcyclohexyl)cyclohexane (4.5 g, 14 mmols).

来源