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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819561Generated: November 1, 2026

Allyl bromide → 2'-Allyloxyacetophenone

https://huagongshe.com/reaction/1819561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactantalpha-HydroxyacetophenoneHCID 68490—
SolventAcetoneHCID 180—
SolventDiethyl EtherHCID 3283—
Product2'-AllyloxyacetophenoneHCID 29944151%

Reaction Steps

To a stirring suspension of 2-hydroxyacetophenone 72 (5 ml, 42 mmol) and potassium carbonate (6.516 g, 47 mmol, 1.1 equ) in acetone (30 ml) was added allyl bromide (4 ml, 46 mmol, 1.1 equ). The reaction was heated to reflux for 20 hours. The reaction was then concentrated in vacuo, taken up in water and extracted into ethyl acetate (2×). The organic layer was then dried (MgSO4) and concentrated in vacuo to give an yellow oil. This was taken up in diethyl ether, washed with 1M potassium hydroxide then dried (MgSO4) and concentrated in vacuo to give 1-(2-allyloxy-phenyl)-ethanone (3.70 g, 51%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601754B2
Source datasetuspto-grants-2009_10
ORD IDord-5104c59827c74c269a7e792afd2fbe8a
Source noteuspto-grants-2009_10