反应 #1552026

反应方程式

t-BuOK

THF

4-(3-Propylcyclopentyl)-cyclohexanone

THF

chloride

THF

→

1-methoxymethylene-4-(3-propylcyclopentyl)cyclohexane

反应条件

后处理

1. 1
   workup.ADDITIONwas added
2. 2
   workup.WAITthe stirring was continued for another 2 hours
3. 3
   萃取was extracted with toluene
4. 4
   workup.ADDITIONafter the addition of water (200 ml) The resulting organic layer
5. 5
   洗涤was washed with water
6. 6
   干燥dried over anhydrous sulfate
7. 7
   浓缩the toluene was concentrated to a volume of about 100 ml under reduced pressure
8. 8
   workup.ADDITIONThe concentrate was poured into n-hexane (500 ml) and solids
9. 9
   过滤deposited were filtered off
10. 10
    workup.DISTILLATIONThe solvent of the resulting solution was distilled off under reduced pressure
11. 11
    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 methoxymethyltriphenylphophnium chloride (29.3 g) in a reaction vessel under an atmosphere of nitrogen, and the solution was cooled to −15° C. t-BuOK (10.5 g) in a THF (50 ml) solution was added, and the stirring was continued for another 1 hour. 4-(3-Propylcyclopentyl)-cyclohexanone (15.0 g) in a THF (50 ml) solution was added dropwise, and the stirring was continued for another 2 hours. The reaction mixture was warmed to room temperature and was extracted with toluene after the addition of water (200 ml) The resulting organic layer was washed with water and dried over anhydrous sulfate, and the toluene was concentrated to a volume of about 100 ml under reduced pressure. The concentrate was poured into n-hexane (500 ml) and solids deposited were filtered off. The solvent of the resulting solution was distilled off under reduced pressure, and the residue was purified by silica gel chromatography (eluent: ethyl acetate/n-heptane=1/9 by volume) to give 1-methoxymethylene-4-(3-propylcyclopentyl)cyclohexane (17.0 g).

来源