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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746333Generated: October 30, 2026

Allyl bromide → 4-(allyloxy)-3-bromobenzaldehyde

https://huagongshe.com/reaction/746333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-4-hydroxybenzaldehydeHCID 76308—
SolventAcetoneHCID 180—
Product4-(allyloxy)-3-bromobenzaldehydeHCID 2716613—

Reaction Steps

3-Bromo-4-hydroxybenzaldehyde (20.1 g, 0.100 mol) and allyl bromide (14.5 g, 0.120 mol) were heated under reflux together with potassium carbonate (20.7 g, 0.150 mol) in 150 ml acetone (abs.) for 8 hours. After cooling, the solid was filtered off and washed with acetone. After complete concentration of the organic phase, there was obtained an oily residue that was used directly in the second step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393367B2
Source datasetuspto-grants-2008_07
ORD IDord-495f487bedfe4f41ae76334d5dcc0546
Source noteuspto-grants-2008_07