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HRID 1528045作成日:2026年10月25日

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

https://huagongshe.com/reaction/1528045

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物4-Fluorobenzoyl chlorideHCID 67879—
反応物2-Methoxy-1-(2,4,6-trihydroxyphenyl)ethanoneHCID 643400—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒TolueneHCID 1140—
生成物2-(4-fluorophenyl)-5,7-dihydroxy-3-methoxy-4H-benzopyran-4-oneHCID 547001281.9%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09090583B2
出典データセットuspto-grants-2015_07
ORD IDord-23ab95caa38544ca903a9f4f46ca5562
出典メモuspto-grants-2015_07