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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 986481생성일: 2026년 10월 25일

Piperidine → 2-(3,5-Dibromo-4-hydroxyphenyl)-6-hydroxy-3-methyl-4H-1-benzopyran-4-one

https://huagongshe.com/reaction/986481

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물Potassium HydroxideHCID 14797—
반응물3,5-Dibromo-4-HydroxybenzaldehydeHCID 18100—
반응물BromineHCID 24408—
반응물2',5'-DihydroxypropiophenoneHCID 70312—
반응물3',5'-Dibromo-6,4'-dihydroxy-3-methylflavanoneHCID 13650818—
반응물3,3',5'-Tribromo-6,4'-dihydroxy-3-methylflavanoneHCID 21283899—
용매EthanolHCID 702—
용매ChloroformHCID 6212—
용매1,4-DioxaneHCID 31275—
생성물2-(3,5-Dibromo-4-hydroxyphenyl)-6-hydroxy-3-methyl-4H-1-benzopyran-4-oneHCID 128600—

반응 단계

1.6 g of bromine in 6 ml of chloroform are added dropwise to a solution of 4.12 g of 3',5'-dibromo-6,4'-dihydroxy-3-methylflavanone (m.p. 200°-202°; obtainable by reaction of 2,5-dihydroxypropiophenone with 3,5-dibromo-4-hydroxybenzaldehyde in boiling ethanol in the presence of piperidine) in 55 ml of dioxane while stirring and irradiating (500 watt Agaphot lamp). The mixture is stirred for a further 30 minutes while cooling and irradiating, the usual working-up is carried out, and the resulting crude 3,3',5'-tribromo-6,4'-dihydroxy-3-methylflavanone is dissolved in 100 ml of ethanol. 15 ml of 10% aqueous potassium hydroxide solution are added, and the mixture is boiled for 5 minutes, cooled, poured on to ice and the usual working-up is carried out. 3',5'-Dibrom-6,4'-dihydroxy-3-methylflavone ("D") is obtained, m.p. 264°-265°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04713465
출처 데이터셋uspto-grants-1987_12
ORD IDord-d4c6203d4710429b8fc2774f31ac37aa
출처 메모uspto-grants-1987_12