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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 370566생성일: 2026년 10월 26일

Methyl (+/-)-3-methyl-1-trichloromethyl-2-butenyl diazomalonate → Methyl 4-trichloromethyl-6,6-dimethyl-2-oxo-3-oxabicyclo[3.1.0]hexane-1-carboxylate

https://huagongshe.com/reaction/370566

반응식

참여 물질

역할이름HCID투입량
반응물Methyl (+/-)-3-methyl-1-trichloromethyl-2-butenyl diazomalonateHCID 53809386—
촉매CopperHCID 23978—
용매OctaneHCID 356—
용매Ethyl AcetateHCID 8857—
생성물Methyl 4-trichloromethyl-6,6-dimethyl-2-oxo-3-oxabicyclo[3.1.0]hexane-1-carboxylateHCID 1252524696%

반응 단계

To a refluxing suspension of copper powder (6.6 g, 0.104 mole) in 320 ml of n-octane was added dropwise in one hour a solution of methyl (±)-3-methyl-1-trichloromethyl-2-butenyl diazomalonate (6.6 g, 0.02 mole, prepared as described above for the ethyl ester) in 80 ml of n-octane. The reaction mixture was heated for 21/2 hours under reflux and then filtered while hot. The n-octane was evaporated from the filtrate under vacuum to produce a residue which was dissolved in ethyl acetate. The solution was washed successively with aqueous 1N hydrochloric acid, aqueous sodium bicarbonate, and aqueous sodium chloride. After drying the solution over magnesium sulfate, the ethyl acetate was removed by evaporation, yielding methyl (±)-4-trichloromethyl-6,6-dimethyl-2-oxo-3-oxabicyclo[3.1.0]hexane-1-carboxylate (5.77 g, 96% yield) as an oil. Trituration of the oil with ether afforded the crystalline lactone; mp, 118°-120°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04526987
출처 데이터셋uspto-grants-1985_07
ORD IDord-db5b7924b9a14e6698f6b6f401ec2b58
출처 메모uspto-grants-1985_07