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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909508Generated: October 30, 2026

Benzyl Chloride → 4-(Benzyloxy)-3,5-difluorobenzaldehyde

https://huagongshe.com/reaction/1909508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-Difluoro-4-hydroxybenzaldehydeHCID 10192584—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(Benzyloxy)-3,5-difluorobenzaldehydeHCID 15714026—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 3,5-difluoro-4-hydroxybenzaldehyde (6) (8.26 g, 52.2 mmol), and potassium carbonate (14.4 g, 104.4 mmol) in dimethylformamide (100 mL) was added benzyl chloride (7.2 mL, 62.7 mmol) and stirred overnight at 50° C. The reaction was diluted with water and extracted with ethyl acetate (3×75 mL). The organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel (0-100% EtOAc in hexanes) to afford 4-(benzyloxy)-3,5-difluorobenzaldehyde (7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598374B2
Source datasetuspto-grants-2013_12
ORD IDord-0b34c01daecf4ae99f5e0a413c8d3ca0
Source noteuspto-grants-2013_12