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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40749Generated: October 28, 2026

4-Fluorophenol → 3-Bromo-5-(4-fluorophenoxy)benzonitrile

https://huagongshe.com/reaction/40749

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-5-fluorobenzonitrileHCID 2783330—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
Product3-Bromo-5-(4-fluorophenoxy)benzonitrileHCID 59588063—

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 4-fluorophenol (0.3 g, 2.7 mmol), 3-bromo-5-fluorobenzonitrile (0.53 g, 2.7 mmol), K2CO3 (1.1 g, 8.0 mmol) in N,N-dimethylacetamide (3 mL) was heated to 160° C. for 3 hr. The reaction mixture was cooled to room temperature and diluted with EtOAc and water. The organic layer was separated, dried (MgSO4), concentrated, and purified by chromatography on silica gel (EtOAc/hexanes) to afford 3-bromo-5-(4-fluorophenoxy)benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530480B2
Source datasetuspto-grants-2013_09
ORD IDord-bed3cd8e8a5b4c08b42837b1b89537c6
Source noteuspto-grants-2013_09