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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705838Generated: October 31, 2026

4-Fluorophenol → 4-(4-Fluorophenoxy)benzaldehyde

https://huagongshe.com/reaction/705838

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
ReactantPotassium CarbonateHCID 11430—
Reactant4-FluorobenzaldehydeHCID 68023—
SolventDimethylformamideHCID 6228—
Product4-(4-Fluorophenoxy)benzaldehydeHCID 385680284.3%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a solution of 4-fluorophenol (10 g, 89 mmol) and 4-fluorobenzaldehyde (11.07 g, 89 mmol) in DMF (200 mL) was added K2CO3 (13.33 g, 96 mmol). The mixture was heated at 140° C. for 4 h. After cooling to room temperature, the mixture was poured into of ice water (300 mL), and left stand overnight. The solid was collected by filtration, washed with water, re-dissolved in EA (200 mL) and washed with brine (100 mL). The organic phase was dried with sodium sulfate, filtered and concentrated to afford the title compound (17 g, 75 mmol, 84% yield) as yellow solid. LCMS: rt=1.52 min, [M+H+]=217

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174968B2
Source datasetuspto-grants-2015_11
ORD IDord-8bddd63461a64eac9ef862a21424f725
Source noteuspto-grants-2015_11