돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127033생성일: 2026년 10월 26일

3-Methyl-1-trichloromethyl-2-butenyl diazoacetate → 4-Trichloromethyl-6,6-dimethyl-2-oxo-3-oxabicyclo[3.1.0]hexane

https://huagongshe.com/reaction/127033

반응식

참여 물질

역할이름HCID투입량
반응물3-Methyl-1-trichloromethyl-2-butenyl diazoacetateHCID 54224363—
촉매Bis(pentane-2,4-dione-kappa~2~O~2~,O~4~)copperHCID 45052134—
용매Diethyl EtherHCID 3283—
용매1,4-DioxaneHCID 31275—
생성물4-Trichloromethyl-6,6-dimethyl-2-oxo-3-oxabicyclo[3.1.0]hexaneHCID 1252521856.5%

반응 단계

To a refluxing solution of cupric acetylacetonate (0.07 g, 0.27 mole) in 70 ml of dioxane was added drop-dropwise over a 31/2 hour period, under an argon atmosphere, a solution of (±)-3-methyl-1-trichloromethyl-2-butenyl diazoacetate (1.09 g, 0.004 moles) and cupric acetylacetonate (0.007 g, 0.027 mmole) in 10 ml of dioxane. The reaction mixture was then heated under reflux for one hour and evaporated to dryness, yielding a residue which was dissolved in ether. The ethereal solution was washed successively with two portions of aqueous 1 N hydrochloric acid, two portions of aqueous sodium bicarbonate, and twice with saturated aqueous sodium chloride. After drying the solution over magnesium sulfate, the ether was evaporated to afford a pale yellow oil, which was purified by column chromatography on a silica gel column using a 9/1 mixture of n-hexane/ethyl acetate as the eluant, to give (±)-4-trichloromethyl-6,6-dimethyl-2-oxo-3-oxabicyclo[3.1.0]hexane (0.55 g, 53% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04254282
출처 데이터셋uspto-grants-1981_03
ORD IDord-a24e740ee3754eeca22a32f79503d176
출처 메모uspto-grants-1981_03