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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 66079생성일: 2026년 10월 24일

Water → 2-hydroxy-9-methoxy-5-methyl-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one

https://huagongshe.com/ko/reaction/66079

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium periodateHCID 516896—
반응물7-Hydroxy-8-methoxy-4-methyl-6-(prop-2-en-1-yl)-2H-1-benzopyran-2-oneHCID 21814502—
촉매Osmium TetroxideHCID 30318—
용매MethanolHCID 887—
생성물2-hydroxy-9-methoxy-5-methyl-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-oneHCID 20380227—

반응 단계

A solution of 2.0 g (8.12 mmols) of 6-allyl-7-hydroxy-8-methoxy-4-methylcoumarin in 20 ml of methanol was treated (mechanical stirring) with 10 ml of water, 5.0 g potassium periodate, and 1.0 ml of a 10% aqueous solution of osmium tetroxide (10 mg/ml). After 3.5 hrs, the mixture was partitioned between water/methylene chloride. The aqueous phase was further extracted with methylene chloride. The organic extracts were dried and evaporated to yield 2-hydroxy-9-methoxy-5-methyl-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one. The compound was dissolved in 40 ml of 98% formic acid and heated under reflux for 1.0 hr. The solution was cooled and evaporated to dryness. The residue was chromatographed over silica, eluting with ethyl acetate/benzene, 1:4, to afford pure 9-methoxy-5-methyl-7H-furo[3,2-g][1]benzopyran-7-one, m.p. 167°-168° (ethanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04130568
출처 데이터셋uspto-grants-1978_12
ORD IDord-7e625edc8b3846789c622aabd8df2edf
출처 메모uspto-grants-1978_12