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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433165Generated: November 2, 2026

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

https://huagongshe.com/reaction/1433165

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2',4'-DihydroxyacetophenoneHCID 6990—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
SolventAcetonitrileHCID 6342—
Product1-(2,4-Bis(benzyloxy)phenyl)ethanoneHCID 31946978.2%

Reaction Steps

Benzyl bromide (35.6 mL, 0.3 mol) was added to a suspension of 2,4-dihydroxyacetophenone (15 g, 0.1 mol) and potassium carbonate (41.4 g, 0.3 mol) in acetonitrile (150 mL) and the mixture stirred overnight. After concentration to dryness, the residues were resuspended in dichloromethane (100 mL) and washed with water (100 mL). The organic phase was dried over magnesium sulphate and concentrated. Trituration with hexanes, filtration and drying in vacuo gave 1-(2,4-Bis-benzyloxyphenyl)-ethanone as a white powder (26 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612201B2
Source datasetuspto-grants-2009_11
ORD IDord-212986c9f09d4442b78e2ee936d40c87
Source noteuspto-grants-2009_11