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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl (+/-)-3-methyl-1-trichloromethyl-2-butenyl diazomalonate | HCID 53809386 | — |
| 촉매 | Copper | HCID 23978 | — |
| 용매 | Octane | HCID 356 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | Methyl 4-trichloromethyl-6,6-dimethyl-2-oxo-3-oxabicyclo[3.1.0]hexane-1-carboxylate | HCID 12525246 | 96% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04526987 |
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| 출처 데이터셋 | uspto-grants-1985_07 |
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| ORD ID | ord-db5b7924b9a14e6698f6b6f401ec2b58 |
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| 출처 메모 | uspto-grants-1985_07 |
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