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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 223794생성일: 2026년 10월 26일

Diiodomethane → Ethyl [(5,6-dichloro-9a-cyclopropyl-3-oxo-1,2,9,9a-tetrahydro-3H-fluoren-7-yl)oxy]acetate

https://huagongshe.com/reaction/223794

반응식

참여 물질

역할이름HCID투입량
반응물DiiodomethaneHCID 6346—
반응물Ethyl [(5,6-dichloro-3-oxo-9a-vinyl-1,2,9,9a-tetrahydro-3H-fluoren-7-yl)oxy]acetateHCID 86738256—
촉매Zinc copper coupleHCID 10290809—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물Ethyl [(5,6-dichloro-9a-cyclopropyl-3-oxo-1,2,9,9a-tetrahydro-3H-fluoren-7-yl)oxy]acetateHCID 86738255—

반응 단계

A mixture of the zinc-copper couple, prepared as described above, (48 gm.) and methylene iodide (37.5 gm.) in tetrahydrofuran (300 ml.) is heated under reflux in a nitrogen atmosphere for an hour. Ethyl [(5,6-dichloro-3-oxo-9a-vinyl-1,2,9,9a-tetrahydro-3H-fluoren-7-yl)oxy]-acetate (8.2 gm., 0.02 mole) is added to the cooled mixture and stirring continued at 25° C. for 24 hours. The mixture is diluted with toluene (200 ml.), filtered and the filtrate is washed successively with saturated aqueous solutions of ammonium chloride and sodium bicarbonate and then with water. The organic lager is dried over anhydrous magnesium sulfate and the solvent removed using a rotary evaporator at reduced pressure. The residue is purified by column chromatography using a silica-gel column to give ethyl [(5,6-dichloro-9a-cyclopropyl-3-oxo-1,2,9,9a-tetrahydro-3H-fluoren-7-yl)oxy]-acetate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04356313
출처 데이터셋uspto-grants-1982_10
ORD IDord-d3a1e9862eb24150ac83cd257af94940
출처 메모uspto-grants-1982_10