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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29881Generated: October 26, 2026

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

https://huagongshe.com/reaction/29881

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
Reactant1-Fluoro-3-nitrobenzeneHCID 9823—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylamineHCID 674—
Product3-(4-Fluorophenoxy)anilineHCID 2350601591.2%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423043B2
Source datasetuspto-grants-2008_09
ORD IDord-2b2c63fa300748dea9d913c55c851a3d
Source noteuspto-grants-2008_09