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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247538Generated: October 30, 2026

Acetone → 1-[5-(Benzyloxy)-2-hydroxyphenyl]ethan-1-one

https://huagongshe.com/reaction/1247538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantBenzyl BromideHCID 7498—
Reactant2-AcetylhydroquinoneHCID 10279—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
Product1-[5-(Benzyloxy)-2-hydroxyphenyl]ethan-1-oneHCID 1287092841.1%

Reaction Steps

2,5-dihydroxyacetophenone (5.00 g, 0.0329 mol), benzyl bromide (3.72 ml, 0.031 mol), potassium carbonate (4.31 g, 0.031 mol) and acetone (150 ml) were added to a 500 ml round bottom flask. The reaction mixture was heated overnight at reflux and then was cooled to ambient temperature. When cool, deionized water (150 ml) was added to the reaction mixture and the reaction mixture was extracted three times with 100 ml portions of diethyl ether. The combined ether layers were dried with sodium sulfate and concentrated in vacuo yielding a dark solid. This dark solid was recrystallized from 50:50 (ethanol:water) yielding 3.09 g of 2-hydroxy-5-benzyloxyacetophenone as yellow needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129274B1
Source datasetuspto-grants-2006_10
ORD IDord-37baf79271b84f35b004bdd0e52c7c6b
Source noteuspto-grants-2006_10