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HRID 2232471作成日:2026年10月25日

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

https://huagongshe.com/reaction/2232471

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物Potassium HydroxideHCID 14797—
反応物3,5-Dibromo-4-HydroxybenzaldehydeHCID 18100—
反応物BromineHCID 24408—
反応物2',5'-DihydroxypropiophenoneHCID 70312—
反応物3',5'-Dibromo-6,4'-dihydroxy-3-methylflavanoneHCID 13650818—
反応物3,3',5'-Tribromo-6,4'-dihydroxy-3-methylflavanoneHCID 21283899—
溶媒EthanolHCID 702—
溶媒ChloroformHCID 6212—
溶媒1,4-DioxaneHCID 31275—
生成物2-(3,5-Dibromo-4-hydroxyphenyl)-6-hydroxy-3-methyl-4H-1-benzopyran-4-oneHCID 128600—

反応手順

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°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04788215
出典データセットuspto-grants-1988_11
ORD IDord-5dc88054038448fc8a387db75cb92ee5
出典メモuspto-grants-1988_11