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HRID 225974作成日:2026年10月27日

Potassium Iodide → 4-(3-Phenoxypropoxy)-7H-furo(3,2-g)(1)benzopyran-7-one

https://huagongshe.com/reaction/225974

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物Benzene, (3-bromopropoxy)-HCID 68522—
反応物BergaptolHCID 5280371—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物4-(3-Phenoxypropoxy)-7H-furo(3,2-g)(1)benzopyran-7-oneHCID 11551761—

反応手順

700 mg (3.5 mmol) of 5-hydroxypsoralen and 750 mg (3.5 mmol) of 3-phenoxypropyl bromide were refluxed in 30 ml of 2-butanone in the presence of an excess of anhydrous potassium carbonate (3.0 g) and catalytic amounts of potassium iodide for 36 hours. The progress of the reaction was monitored by thin layer chromatography. After 36 hours the reaction mixture was concentrated under reduced pressure. The oily residue was cooled and diluted with water. The aqueous solution was then acidified with concentrated hydrochloric acid to pH 1. The slurry was stirred for 15-20 min and extracted with 3×30 ml of dichloromethane. The dichloromethane layer was extracted with 25 ml of 1% sodium hydroxide to separate the un-reacted 5-hydroxypsoralen. The dichloromethane layer was washed with 30 ml of 2% hydrochloric acid, dried over anhydrous sodium sulfate and concentrated. The resulting oily residue was dissolved in methanol, treated with charcoal and re-crystallized from a methanol-ethyl acetate (10:90) mixture.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557138B2
出典データセットuspto-grants-2009_07
ORD IDord-edb4e9a0329341b984779280a5ca5ea8
出典メモuspto-grants-2009_07