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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34470생성일: 2026년 10월 26일

Acetic Acid → Ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propanoate

https://huagongshe.com/reaction/34470

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Bromocresol GreenHCID 6451—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물Ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propenoateHCID 54507081—
용매EthanolHCID 702—
생성물Ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propanoateHCID 20129780—

반응 단계

A mixture of ethyl 2-cyano-3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)propenoate (19.8 g, 0.63 mole) in ethanol (500 mL) under nitrogen was treated with acetic acid (4 mL) and a trace of bromocresol green and heated to reflux. Heating was discontinued and sodium cyanoborohydride (4.4 g, 0.07 mole) in ethanol (100 mL) was co-added with additional acetic acid (11 mL). The mixture was stirred under nitrogen for 2 hr, acetic acid (10 mL) added and the ethanol removed under reduced pressure. The resultant yellow solid was taken up in ethyl acetate (250 mL) and successively extracted with water (125 mL), saturated sodium bicarbonate (3×100 mL) and water (100 mL), then dried over magnesium sulfate. The volatiles were removed under reduced pressure to leave an amber oil, 18.22 g (91.4%) which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04761475
출처 데이터셋uspto-grants-1988_08
ORD IDord-62b182c93158406b8248468834a06f6a
출처 메모uspto-grants-1988_08