Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29881Erstellt: 26. Oktober 2026

4-Fluorophenol → 3-(4-Fluorophenoxy)aniline

https://huagongshe.com/reaction/29881

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-FluorophenolHCID 9732—
Edukt1-Fluoro-3-nitrobenzeneHCID 9823—
EduktPotassium CarbonateHCID 11430—
LösungsmittelDimethylamineHCID 674—
Produkt3-(4-Fluorophenoxy)anilineHCID 2350601591,2%

Reaktionsschritte

Alternatively, 3-(4-fluoro-phenoxy)-phenylamine was prepared by a two-step procedure by heating a suspension of m-fluoronitrobenzene (4.06 g, 28.7 mmol), p-fluorophenol (3.21 g, 28.6 mmol) and K2CO3 (8.13 g, 58.8 mmol) in DMA (dimethylamine) (60 mL) at 150° C. for 3 hours. The brown reaction mixture was concentrated to one-quarter original volume, diluted with ethyl acetate (220 mL) and washed successively with water (220 mL), 1N NaOH (220 mL) and brine (220 mL). The organic layer was dried (MgSO4) and the solvent removed in vacuo to afford the diphenylether (5.30 g, 80%) as a brown oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423043B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-2b2c63fa300748dea9d913c55c851a3d
Quellennotizuspto-grants-2008_09