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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985817Generated: November 2, 2026

Hydrochloric Acid → 4-Benzyloxy-3-hydroxybenzaldehyde

https://huagongshe.com/reaction/1985817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl BromideHCID 7498—
Reactant3,4-DihydroxybenzaldehydeHCID 8768—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product4-Benzyloxy-3-hydroxybenzaldehydeHCID 561369—

Reaction Steps

3,4-Dihydroxybenzaldehyde (21.6 g) and potassium carbonate (21.56 g) were suspended in N,N-dimethylformamide (200 mL). To the mixture was added dropwise benzylbromide (18.5 mL) under ice-cooling, and the mixture was stirred at room temperature for 16 hours. To the reaction mixture was added dropwise 2 mol/L hydrochloric acid (400 mL), and the resulting mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the obtained residue was purified by column chromatography on silica gel (eluent: ethyl acetate/hexane=1/5) to give the title compound (19.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547680B2
Source datasetuspto-grants-2009_06
ORD IDord-4c0f1c2b26ae4c5687489ff52e57e1df
Source noteuspto-grants-2009_06