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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7472Generated: October 25, 2026

Acetovanillone → 1-(4-Benzyloxy-3-methoxy-phenyl)-ethanone

https://huagongshe.com/reaction/7472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetovanilloneHCID 2214—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-(4-Benzyloxy-3-methoxy-phenyl)-ethanoneHCID 9921599%

Reaction Steps

The starting material, 4-benzyloxy-3-methoxyacetophenone, was obtained by heating a solution of 4-hydroxy-3-methoxyacetophenone (20 g, 0.12 mol), benzyl bromide (15.7 ml, 0.13 mol) and potassium carbonate (49.8 g, 0.36 mol), in DMF (400 ml) at 40° C. overnight. After cooling, the mixture was diluted with water, acidified to approximately pH3 and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4) and the solvent evaporated. The residue was purified by flash chromatography using petroleum ether/ethyl acetate (8/2 followed by 65/35) as eluent to give 4-benzyloxy-3-methoxyacetophenone (30.3 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087602B2
Source datasetuspto-grants-2006_08
ORD IDord-5361ab59f70448ae8738fc7abac188e4
Source noteuspto-grants-2006_08