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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658805Generated: October 30, 2026

4-Hydroxybenzaldehyde → 4-[(3-Fluorophenyl)methoxy]benzaldehyde

https://huagongshe.com/reaction/658805

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
Reactant3-Fluorobenzyl chlorideHCID 9974—
ReactantSodium HydroxideHCID 14798—
SolventEthanolHCID 702—
Product4-[(3-Fluorophenyl)methoxy]benzaldehydeHCID 880119101.8%

Reaction Steps

Accordingly, 3-fluorobenzyl chloride (14.5 g, 100 mmol) is added under stirring and under nitrogen atmosphere to a solution of 4-hydroxybenzaldehyde (12.2 g, 100 mmol) and of NaOH (4.0 g, 100 mmol) in ethanol (100 mL). The mixture is gradually heated in 25 minutes to reflux and stirred at reflux temperature for 6 hours and 20 minutes. The reaction mixture is filtrated and then concentrated at reduced pressure to obtain 4-(3-fluoro-benzyloxy)benzaldehyde (23.43 g) as a yellow solid residue. Dichloromethane (250 mL) is added to the residue, the insoluble is filtered and the resulting solution is concentrated under reduced pressure to provide 4-(3-fluorobenzyloxy)benzaldehyde as a yellow solid, in 80.4% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076515B2
Source datasetuspto-grants-2011_12
ORD IDord-3bc27e15950b4f57831619399a611f63
Source noteuspto-grants-2011_12