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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646498Generated: October 30, 2026

2',4'-Dihydroxyacetophenone → 1-(2,4-Bis(benzyloxy)phenyl)ethanone

https://huagongshe.com/reaction/646498

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2',4'-DihydroxyacetophenoneHCID 6990—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
SolventAcetonitrileHCID 6342—
Product1-(2,4-Bis(benzyloxy)phenyl)ethanoneHCID 319469—

Reaction Steps

Potassium carbonate (2.5 eq) was added to a solution of 2′,4′-dihydroxyacetophenone (1 eq) in acetonitrile (400 mL), and the suspension stirred at room temperature. Benzyl bromide (2.5 eq) was added drop wise over 10 minutes and the mixture heated at reflux for 18 hours. The mixture was cooled and evaporated in vacuo to give slurry. The slurry was partitioned between water and ethyl acetate, and the layers were separated. The aqueous layer was further extracted with dichloromethane and the organic extracts were combined, dried (MgSO4) and evaporated in vacuo. The product was triturated with hexane, filtered and washed with cold hexane and dried in vacuo at 45° C. to give 1-(2,4-Bis-benzyloxy-phenyl)-ethanone as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705027B2
Source datasetuspto-grants-2010_04
ORD IDord-1b81bbb7e80e47d18334ef91aef8b988
Source noteuspto-grants-2010_04