돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225979생성일: 2026년 10월 26일

Potassium Iodide → 4-(4-Pentynyloxy)-7H-furo[3,2-g][1]benzopyran-7-on

https://huagongshe.com/reaction/225979

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물1-Pentyne, 5-chloro-HCID 84308—
반응물BergaptolHCID 5280371—
용매AcetonitrileHCID 6342—
생성물4-(4-Pentynyloxy)-7H-furo[3,2-g][1]benzopyran-7-onHCID 11659029—

반응 단계

500 mg (2.473 mmol) of 5-hydroxypsoralen and 405.85 mg (3.957 mmol) of 5-chloro-1-pentyne were refluxed in 30 ml of acetonitrile in the presence of an excess of anhydrous potassium carbonate (2.0 gm) and catalytic amounts of potassium iodide for 24 hours. The progress of the reaction was monitored by thin layer chromatography. After 24 hours the reaction mixture was concentrated under reduced pressure. The oily residue was cooled, diluted with water and acidified with concentrated hydrochloric acid to pH 1. The aqueous phase was extracted with dichloromethane. The dichloromethane phase was extracted with 25 ml of 1% sodium hydroxide to separate the un-reacted 5-hydroxypsoralen. The dichloromethane phase was washed with acidic water and then with water to pH˜6-7. The organic phase was then dried over anhydrous sodium sulphate and concentrated to dryness. The residue was dissolved in methanol, decolorized with charcoal and re-crystallized from methanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557138B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-166a04a00c314d4eb06eca2fbb449ce3
출처 메모uspto-grants-2009_07