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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1528045생성일: 2026년 10월 25일

Potassium Carbonate → 2-(4-fluorophenyl)-5,7-dihydroxy-3-methoxy-4H-benzopyran-4-one

https://huagongshe.com/reaction/1528045

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-Fluorobenzoyl chlorideHCID 67879—
반응물2-Methoxy-1-(2,4,6-trihydroxyphenyl)ethanoneHCID 643400—
촉매Tetrabutylammonium BromideHCID 74236—
용매TolueneHCID 1140—
생성물2-(4-fluorophenyl)-5,7-dihydroxy-3-methoxy-4H-benzopyran-4-oneHCID 547001281.9%

반응 단계

Under nitrogen atmosphere, 2-methoxy-1-(2,4,6-trihydroxyphenyl)ethanone (60 mg, 303.03 mmol), anhydrous potassium carbonate powder (250.9 g, 1.82 mmol), TBAB (tetrabutyl ammonium bromide, 145.9 mg, 454.52 mmol) and 4-fluorobenzoyl chloride (95.8 mg, 606 mmol) were dissolved in toluene (1200 mL), and refluxed for 6 hours. After cooling, toluene was removed, and then water (500 mL) was added. The aqueous solution was extracted with dichloromethane. The combined organic phase was washed with water and saturated brine, and dried over anhydrous sodium sulfate. A brown residue was obtained after removal of solvent. The residue was dissolved in a 5% potassium carbonate aqueous solution and heated to reflux for 2 hr. After cooling to ambient temperature, the mixture was acidified to pH 6 with 1N HCl solution, and extracted with dichloromethane three times. The combined organic phase was dried over anhydrous sodium sulfate, and the solvent was removed. The crude product was purified by silica gel column chromatography (eluent:ethyl acetate/petroleum ether, 1:5) and recrystallized in ethanol to give the desired compound (75 g, yield 81.9%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09090583B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-23ab95caa38544ca903a9f4f46ca5562
출처 메모uspto-grants-2015_07