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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460020Generated: October 25, 2026

Benzyl Bromide → Ethanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]-

https://huagongshe.com/reaction/460020

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4'-Hydroxy-3'-methylacetophenoneHCID 70135—
SolventAcetonitrileHCID 6342—
ProductEthanone, 1-[3-methyl-4-(phenylmethoxy)phenyl]-HCID 12969325—

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 4-hydroxy-3-methylacetophenone (5.0 g) in dry acetonitrile (50 ml) was treated with potassium carbonate (5.06 g) and benzyl bromide (3.96 ml) and the reaction mixture heated at 40° C. After 3 hours the reaction was allowed to cool and was concentrated. The residue was partitioned between water and ethyl acetate; the aqueous layer separated and extracted twice more with ethyl acetate. The organic solutions were combined and were dried with brine and over magnesium sulfate and concentrated to give the title compound as a colourless oil

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196107B2
Source datasetuspto-grants-2007_03
ORD IDord-da235d1cfd0447f28bdf62d1f7e867b5
Source noteuspto-grants-2007_03