反应 #1463482

反应方程式

2-(1,3-dioxan-2-yl)ethyltriphenylphosphonium bromide

tetrahydrofuran

tetrahydrofuran

(4-(4-propylphenyl)phenyl)cyclohexanone

potassium t-butoxide

→

4-(4-propylphenyl)phenylcyclohexane

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The resulting reaction mixture
4. 4
   其他up to room temperature
5. 5
   其他for one hour
6. 6
   workup.STIRRINGstirring for one hour
7. 7
   workup.STIRRINGfurther stirring
8. 8
   其他the reaction liquid for 5 hours
9. 9
   workup.ADDITIONafter completion of the dropwise addition
10. 10
    过滤filtering off
11. 11
    浓缩concentrating the filtrate under reduced pressure
12. 12
    其他isolating
13. 13
    其他purifying the resulting pale brown oil by means of silica gel column chromatography

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)ethyltriphenylphosphonium bromide (22.9 g, 50 mmols), followed by adding tetrahydrofuran (100 ml), suspending, stirring the suspension under ice cooling till the liquid temperautre reached 10° C. The resulting reaction mixture is added potassium t-butoxide (5.6 g, 50 mmols), followed by elevating the temperature up to room temperature under ice cooling for one hour, stirring for one hour, dropwise adding a tetrahydrofuran (100 ml) solution of (4-(4-propylphenyl)phenyl)cyclohexanone (14.0 g, 48 mmols) over 30 minutes from the dropping funnel, further stirring the reaction liquid for 5 hours after completion of the dropwise addition, adding ether (200 ml), allowing to stand for one hour, filtering off deposited insoluble substance, concentrating the filtrate under reduced pressure and isolating and purifying the resulting pale brown oil by means of silica gel column chromatography, to obtain 1-(2-(1,3-dioxan-2-yl)ethylidene)-4-(4-(4-propylphenyl)phenylcyclohexane.

来源