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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985834Generated: November 1, 2026

Hydrochloric Acid → 2-Benzyloxy-4-cyanobenzaldehyde

https://huagongshe.com/reaction/1985834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Formyl-3-hydroxybenzonitrileHCID 12813648—
SolventDimethylformamideHCID 6228—
Product2-Benzyloxy-4-cyanobenzaldehydeHCID 18973906—

Reaction Steps

4-Formyl-3-hydroxybenzonitrile (4.0 g) and potassium carbonate (3.76 g) were suspended in N,N-dimethylformamide (20 mL). To the reaction mixture was added benzylbromide (3.6 mL), and the mixture was stirred at room temperature for 16 hours. To the reaction mixture was added 1 mol/L hydrochloric acid, and the resulting mixture was extracted with diethyl ether. The organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution and brine successively and dried over anhydrous magnesium sulfate. The filtrate was concentrated under reduced pressure, and the obtained residue was purified by column chromatography on silica gel (ethyl acetate/hexane=1/1) to give the title compound (3.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547680B2
Source datasetuspto-grants-2009_06
ORD IDord-430c30e25103493795672ec87b624abd
Source noteuspto-grants-2009_06