반응 #2446062
ord-8b4057b3f33240f3886eec06264da753
반응 방정식
반응 조건
후처리
- 1온도it was warmed to −40° C.
- 2workup.STIRRINGstirred for another 2.5 hours
- 3온도the mixture was warmed to room temperature
- 4기타The mixture was separated
- 5추출the water layer was extracted with diethyl ether three times
- 6세척the combined organic layer was washed with brine
- 7건조The solution was dried over anhydrous magnesium sulfate
- 8workup.DISTILLATIONthe solvent was distilled off under reduced pressure
- 9기타The residue was purified by silica gel chromatography (eluent: ethyl acetate/n-heptane= 1/20 by volume)
실험 절차
Diethyl ether (800 ml) and tributylphosphine (83 ml) were added to copper iodide (41.4 g) in a reaction vessel under an atmosphere of nitrogen, and the mixture was cooled to −78° C., and then n-butyllithium (1.65 M, a hexane solution) (19 ml) was added dropwise at a temperature of −70° C. or lower. The stirring was continued at −78° C. for 20 minutes, and 2-cyclopentene-1-one (17.0 g) in a diethyl ether (150 ml) solution was added dropwise at a temperature of −70° C. or lower. After the mixture had been stirred at −78° C. for another 20 minutes, it was warmed to −40° C., and stirred for another 2.5 hours. Then, a saturated aqueous solution of ammonium chloride (600 ml) was added at −40° C., and the mixture was warmed to room temperature. The mixture was separated, and the water layer was extracted with diethyl ether three times, and then the combined organic layer was washed with brine. The solution was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (eluent: ethyl acetate/n-heptane= 1/20 by volume) to give 3-butyl-cyclopentanone (15.4 g).