تفاعل #2446065
ord-3a43f35548de4ef582c8547d3d8b561f
معادلة التفاعل
ظروف التفاعل
المعالجة
- 1workup.ADDITIONwas added
- 2workup.WAITthe stirring was continued for another 2 hours
- 3استخلاصwas extracted with toluene
- 4workup.ADDITIONafter the addition of water (200 ml)
- 5غسيلThe resulting organic layer was washed with water
- 6تجفيفdried over anhydrous sulfate
- 7تركيزthe toluene was concentrated to a volume of about 100 ml under reduced pressure
- 8workup.ADDITIONThe concentrate was poured into n-hexane (500 ml) and solids
- 9ترشيحdeposited were filtered off
- 10workup.DISTILLATIONThe solvent of the resulting solution was distilled off under reduced pressure
- 11أخرىthe residue was purified by silica gel chromatography (eluent: ethyl acetate/n-heptane= 1/9 by volume)
الإجراء التجريبي
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).