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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394147Generated: October 31, 2026

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

https://huagongshe.com/reaction/1394147

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
ReactantPotassium CarbonateHCID 11430—
Reactant4-FluorobenzaldehydeHCID 68023—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product4-(4-Fluorophenoxy)benzaldehydeHCID 3856802—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 4-fluorophenol (1.06 g) in anhydrous DMF (10 mL) were added anhydrous potassium carbonate (2.07 g) and 4-fluorobenzaldehyde (1.2 g) at room temperature. The reaction was stirred at 100° C. for 16 h, then cooled to room temperature and diluted with ether. The organic layer was washed with 1N sodium hydroxide, and then with water, dried over sodium sulphate, and concentrated under reduced pressure. The crude aldehyde obtained was purified by flash-column chromatography on silica-gel using 20% EtOAc in hexanes to provide the pure aldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348348B2
Source datasetuspto-grants-2008_03
ORD IDord-4b777751155f492480087b5dd69aa19e
Source noteuspto-grants-2008_03