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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097253Generated: October 30, 2026

Benzyl Bromide → 1-(2,4-Bis(benzyloxy)-5-chlorophenyl)ethanone

https://huagongshe.com/reaction/2097253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(5-Chloro-2,4-dihydroxyphenyl)ethan-1-oneHCID 17245119—
SolventAcetonitrileHCID 6342—
Product1-(2,4-Bis(benzyloxy)-5-chlorophenyl)ethanoneHCID 1796369190%

Reaction Steps

Benzyl bromide (30 mL) was added to a mixture of 1-(5-chloro-2,4-dihydroxy-phenyl)-ethanone (20 g, 0.107 moles) and potassium carbonate (37 g, 2.5 equiv) in acetonitrile (350 mL). The mixture was heated at reflux for 6 hours then allowed to cool and stirred overnight. The mixture was filtered and the solids were washed with dichloromethane (3×100 mL). The combined organic extracts were evaporated in vacuo to leave a pale yellow solid which was triturated with a mixture of hexane (350 mL)/ethyl acetate (15 mL) and filtered to give an off-white solid, 1-(2,4-bis-benzyloxy-5-chloro-phenyl)-ethanone (35.4 g, 90%). 1H NMR (400 MHz) consistent with structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450310B2
Source datasetuspto-grants-2013_05
ORD IDord-6b320a8ab65848508544bf3d869a7569
Source noteuspto-grants-2013_05