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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043215Generated: November 1, 2026

Benzyl Bromide → 6-(Benzyloxy)-2,3-difluorobenzaldehyde

https://huagongshe.com/reaction/1043215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-Difluoro-6-hydroxybenzaldehydeHCID 21221031—
SolventDimethylformamideHCID 6228—
Product6-(Benzyloxy)-2,3-difluorobenzaldehydeHCID 53440898—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 2,3-difluoro-6-hydroxybenzaldehyde (0.93 g), (bromomethyl)benzene (1.11 g) and potassium carbonate (1.22 g) in N,N-dimethylformamide (15 mL) was heated at 70° C. overnight. After cooling to room temperature, the reaction mixture was partitioned between water and ethyl acetate. The organic layer was separated, and the aqueous layer was extracted with additional ethyl acetate three times. The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated. The residue was purified by flash chromatography on silica gel to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557983B2
Source datasetuspto-grants-2013_10
ORD IDord-d589bd2625f5466b949e60fd00af5eff
Source noteuspto-grants-2013_10