Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 370563생성일: 2026년 10월 24일
(+/-)-3-Methyl-1-tribromomethyl-2-butenyl diazoacetate → 4-Tribromomethyl-6,6-dimethyl-2-oxo-3-oxabicyclo[3.1.0]hexane
https://huagongshe.com/ko/reaction/370563
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (+/-)-3-Methyl-1-tribromomethyl-2-butenyl diazoacetate | HCID 53875604 | — |
| 촉매 | Bis(pentane-2,4-dione-kappa~2~O~2~,O~4~)copper | HCID 45052134 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 4-Tribromomethyl-6,6-dimethyl-2-oxo-3-oxabicyclo[3.1.0]hexane | HCID 12525225 | 28% |
반응 단계
To a refluxing solution of cupric acetylacetonate (0.005 g, 0.019 mmole) in 40 ml of toluene was added dropwise over a period of 2.5 hours under an atmosphere of argon gas a solution of (±)-3-methyl-1-tribromomethyl-2-butenyl diazoacetate (0.203 g, 0.005 ml) in 10 ml of toluene. The mixture was then heated under reflux for one hour. After cooling, the reaction mixture was washed successively with two portions of 1N aqueous hydrochloric acid, once with saturated aqueous sodium bicarbonate, and twice with saturated aqueous sodium chloride. After drying over magnesium sulfate, the solution was evaporated to give a yellow oil as the residue. The residue was purified by column chromatography on a silica gel column using 9/1 n-hexane/ethyl acetate as the eluent, yielding (±)-4-tribromomethyl-6,6-dimethyl-2-oxo-3-oxabicyclo[3.1.0]hexane (0.053 g, yield 28%); mp 101°-103° after recrystallization from n-hexane.
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-32ea1d5472ef4db18ec68e2a33fc7766 |
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| 출처 메모 | uspto-grants-1985_07 |
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