Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 65592Erstellt: 23. Oktober 2026

2-Fluorophenol → 2-[4-(2-Fluorophenoxy)phenyl]propionic acid

https://huagongshe.com/de/reaction/65592

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-FluorophenolHCID 9707—
EduktPotassium HydroxideHCID 14797—
Edukt2-(4-Iodophenyl)propanoic acidHCID 15225573—
KatalysatorWaterHCID 962—
KatalysatorCopperHCID 23978—
Produkt2-[4-(2-Fluorophenoxy)phenyl]propionic acidHCID 20559786—

Reaktionsbedingungen

Temperatur180 °C

Reaktionsschritte

2-Fluorophenol (2.35 g.) was fused with potassium hydroxide (1.7 g.) and a few drops of water by heating to 180° C. 2-(4-Iodophenyl)propionic acid (2.76 g.) and copper powder (0.1 g.) were then added and the melt ws heated at 160°-170° C. for 1 hour. The cooled solid was partitioned with methylene chloride (50 ml.) and 2.5N sodium hydroxide (50 ml.). The aqueous layer was acidified with hydrochloric acid, the resulting gum was extracted into ether, and the ether extract was extracted with saturated potassium carbonate solution. This aqueous extract was acidified with hydrochloric acid and the product isolated in ether. After evaporation the resulting solid was purified by preparative layer chromatography using 5% acetic acid/petroleum ether b.p. 62°-68° C. and eluting with ethyl acetate. Recrystallization from petroleum ether b.p. 62°-68° C. gave 2-[4-(2-fluorophenoxy)phenyl]propionic acid, m.p. 106°-108° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04128573
Quelldatensatzuspto-grants-1978_12
ORD IDord-a480ab6c73eb43689a2bfa1d299ef1ed
Quellennotizuspto-grants-1978_12