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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1528045Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1528045

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt4-Fluorobenzoyl chlorideHCID 67879—
Edukt2-Methoxy-1-(2,4,6-trihydroxyphenyl)ethanoneHCID 643400—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelTolueneHCID 1140—
Produkt2-(4-fluorophenyl)-5,7-dihydroxy-3-methoxy-4H-benzopyran-4-oneHCID 547001281,9%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09090583B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-23ab95caa38544ca903a9f4f46ca5562
Quellennotizuspto-grants-2015_07