Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057327Generated: November 4, 2026

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

https://huagongshe.com/reaction/1057327

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 numberUS06514971B1
Source datasetuspto-grants-2003_02
ORD IDord-b075d3c6a13e4618b2e7318ac1de893e
Source noteuspto-grants-2003_02