تفاعل #2446067

معادلة التفاعل

t-BuOK

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1-(3-propylcyclopentyl)-4-vinylcyclohexane

المذيبات

THF

THF

THF

ظروف التفاعل

المعالجة

1. 1
   workup.ADDITIONwas added
2. 2
   استخلاصwas extracted with toluene
3. 3
   workup.ADDITIONafter the addition of water (50 ml)
4. 4
   غسيلThe resulting organic layer was washed with water
5. 5
   تجفيفdried over anhydrous sulfate
6. 6
   تركيزthe solution was concentrated under reduced pressure to a volume of about 50 ml
7. 7
   workup.ADDITIONThe concentrate was poured into n-hexane (200 ml) and solids
8. 8
   ترشيحdeposited were filtered off
9. 9
   workup.DISTILLATIONThe solvent of the resulting solution was distilled off under reduced pressure
10. 10
    أخرىthe residue was purified by silica gel chromatography (eluent: n-heptane)
11. 11
    أخرىpurified by means of a preparative HPLC system, Model PLC-561

الإجراء التجريبي

THF (50 ml) was added to methyltriphenylphosphonium bromide (6.27 g) in a reaction vessel under an atmosphere of nitrogen, and the mixture was cooled to −15° C. t-BuOK (1.97 g) in a THF (20 ml) solution was added, and the stirring was continued for another 1 hour. 4-(3-Propylcyclopentyl)-cyclohexanone4-(3-propylcyclopentyl)cyclohexanecarboaldehyde (3.0 g) in a THF (20 ml) solution was added dropwise and the mixture was stirred for another 2 hours. The reaction mixture was warmed to room temperature and was extracted with toluene after the addition of water (50 ml). The resulting organic layer was washed with water and dried over anhydrous sulfate, and the solution was concentrated under reduced pressure to a volume of about 50 ml. The concentrate was poured into n-hexane (200 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: n-heptane) and then purified by means of a preparative HPLC system, Model PLC-561 made by GL Sciences Inc. to give 1-(3-propylcyclopentyl)-4-vinylcyclohexane (2.0 g).

المصدر