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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660614Generated: October 25, 2026

Water → 1-[2-(Benzyloxy)-6-hydroxyphenyl]ethan-1-one

https://huagongshe.com/reaction/660614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2',6'-DihydroxyacetophenoneHCID 69687—
SolventDimethylformamideHCID 6228—
Product1-[2-(Benzyloxy)-6-hydroxyphenyl]ethan-1-oneHCID 2775187—

Reaction Steps

To a solution of 1-(2,6-dihydroxyphenyl)-ethanone (304 mg, 2 mmol) and benzyl bromide (0.255 mL, 2.1 mmol) in DMF (10 mL) is added K2CO3 (552 mg; 4 mmol) and the mixture is stirred at RT for 18 h. Water is added and the mixture is extracted with EtOAc. The organic phase is washed with water and brine then is dried over sodium sulfate. The solvent is removed under reduced pressure and the residue is purified by flash chromatography using hexane/EtOAc (10:1) as eluent to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084448B2
Source datasetuspto-grants-2011_12
ORD IDord-6934f9b747f54b6fa8d6cf9c529abafd
Source noteuspto-grants-2011_12