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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225974생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/225974

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물Benzene, (3-bromopropoxy)-HCID 68522—
반응물BergaptolHCID 5280371—
용매Methyl Ethyl KetoneHCID 6569—
생성물4-(3-Phenoxypropoxy)-7H-furo(3,2-g)(1)benzopyran-7-oneHCID 11551761—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557138B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-edb4e9a0329341b984779280a5ca5ea8
출처 메모uspto-grants-2009_07