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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690195Generated: October 31, 2026

Allyl bromide → 1-(4-(2-Propen-1-yloxy)phenyl)ethanone

https://huagongshe.com/reaction/1690195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactantalpha-HydroxyacetophenoneHCID 68490—
SolventAcetoneHCID 180—
Product1-(4-(2-Propen-1-yloxy)phenyl)ethanoneHCID 95969100%

Reaction Steps

2-Hydroxyacetophenone (1.36 g, 10.0 mmol) was dissolved in acetone (50 mL). The resultant mixture was added with potassium carbonate (2.76 g, 20.0 mmol) and allylbromide (1.27 mL, 15.0 mmol) at room temperature and heated to reflux for 3 hours. The reaction solution was cooled to room temperature, added with ethyl acetate, and washed with water and brine. The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. The obtained residue was purified using silica-gel column chromatography (n-hexane/ethyl acetate=10/1). 1-(4-(Allyloxy)phenyl)ethanone (1.76 g, 100%) was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153634B2
Source datasetuspto-grants-2012_04
ORD IDord-5d8b4c1c47134fb186791500228b82af
Source noteuspto-grants-2012_04