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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 750551생성일: 2026년 10월 27일

Chlorodifluoromethane → Methyl 9-difluoromethylxanthene-9-carboxylate

https://huagongshe.com/reaction/750551

반응식

참여 물질

역할이름HCID투입량
반응물ChlorodifluoromethaneHCID 6372—
반응물methyl 9H-xanthene-9-carboxylateHCID 699662—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Methyl 9-difluoromethylxanthene-9-carboxylateHCID 68963094—

반응 단계

16.8 g (0.07 mol) of methyl 9-xanthenecarboxylate (obtainable according to step 1.1.a) are dissolved in 300 mL of tetrahydrofuran and 9.1 g (0.077 mol) of potassium tert-butoxide are added batchwise while cooling. Then difluorochloromethane is piped in at 0° C. over a period of 1.5 hours. After all the gas has been piped in, the reaction mixture is left to stand for 72 hours at ambient temperature. The reaction mixture is then diluted with water to a total volume of about 2000 mL, extracted with ethyl acetate, the organic phase is separated off and washed with 5% aqueous sodium carbonate solution. After being extracted again with water, the organic phase is dried over magnesium sulfate and the solvent is removed by distillation. The crude product is purified by chromatography on silica gel (eluent: cyclohexane-ethyl acetate (98:2)) or by recrystallization from cyclohexane. Yield: 5.35 g of white crystals (26% of theoretical yield); melting point: 101° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07405224B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-7d4ce18d309743089513cffe55a4e21e
출처 메모uspto-grants-2008_07