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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 434804생성일: 2026년 10월 25일

Ethanol → 7-Methylcamptothecin

https://huagongshe.com/reaction/434804

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Hydrogen PeroxideHCID 784—
반응물Sulfuric AcidHCID 1118—
반응물CamptothecinHCID 24360—
용매WaterHCID 962—
생성물7-MethylcamptothecinHCID 9799066—

반응 단계

Ferrous sulfate heptahydrate (4.17 g, 15 m-mol) and ethanol (3 ml, 60 m-mol) were dissolved in water (30 ml). Camptothecin (700 mg, 2 m-mol) was suspended in the solution and dissolved therein by adding concentrated sulfuric acid (15 ml) in small portions to the suspension. To the mixture was added dropwise under ice-cooling and agitation a 30% aqueous solution of hydrogen peroxide (1.63 ml, 16 m-mol). After addition of the hydrogen peroxide, the mixture was stirred for 6 hours at room temperature. To the reaction mixture was added ferrous sulfate heptahydrate (2.0 g, 7.2 m-mol) and then was added dropwise under ice-cooling and agitation a 30% aqueous solution of hydrogen peroxide (1 ml, 9.8 m-mol). The agitation was continued for 15 hours at room temperature. To complete the reaction, additional ferrous sulfate heptahydrate (4.2 g, 15 m-mol) and a 30% aqueous solution of hydrogen peroxide (1.5 ml, 14.7 m-mol) were added to the reaction mixture and the whole was stirred for 8 hours at room temperature. The reaction mixture was diluted with ice water (2.5 liters) and extracted with chloroform (3 liters). The chloroform layer was dried with anhydrous magnesium sulfate, filtered and evaporated until dryness under reduced pressure. The residue was purified by way of column chromatography (chloroform) through silica gel (10 g) followed by recrystallization from n-hexane-chloroform whereby 127 mg (17.5%) of the objective compound were obtained as yellow needle crystals. M.P. 280°-281° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04399282
출처 데이터셋uspto-grants-1983_08
ORD IDord-87c61dbde0d841e89aff1195e245ef11
출처 메모uspto-grants-1983_08