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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

반응식

참여 물질

역할이름HCID투입량
반응물(+/-)-3-Methyl-1-tribromomethyl-2-butenyl diazoacetateHCID 53875604—
촉매Bis(pentane-2,4-dione-kappa~2~O~2~,O~4~)copperHCID 45052134—
용매TolueneHCID 1140—
생성물4-Tribromomethyl-6,6-dimethyl-2-oxo-3-oxabicyclo[3.1.0]hexaneHCID 1252522528%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04526987
출처 데이터셋uspto-grants-1985_07
ORD IDord-32ea1d5472ef4db18ec68e2a33fc7766
출처 메모uspto-grants-1985_07