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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606332Generated: October 25, 2026

Propargyl bromide → 1-(2-Hydroxy4-prop-2-ynyloxy-phenyl)-propan-1-one

https://huagongshe.com/reaction/606332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium CarbonateHCID 11430—
Reactant2',4'-DihydroxypropiophenoneHCID 79856—
SolventAcetoneHCID 180—
Product1-(2-Hydroxy4-prop-2-ynyloxy-phenyl)-propan-1-oneHCID 2248283485.5%

Reaction Steps

A mixture of 2′,4′-dihydroxy-propiophenone (24.9 g, 0.15 mol), 3-bromo-propyne (24.2 g, 0.20 mol) and K2CO3 (20.7 g, 0.15 mol) in acetone (500 mL) was refluxed for 12 h. The reaction mixture was allowed assume room temperature and the precipitate was removed by filtration. The filtrate was concentrated under reduced pressure. The crude product was purified by column chromatography (silica gel, 0→2% MeOH in H2O), to give 26.2 g (85%) of 1-(2-hydroxy-4-prop-2-ynyloxy-phenyl)-propan-1-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915295B2
Source datasetuspto-grants-2011_03
ORD IDord-0ce989aeabc848adb35e3987274e3c7b
Source noteuspto-grants-2011_03