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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412166Generated: October 25, 2026

Allyl bromide → 2-Benzyloxy-5-[(2-propenyl)oxy]benzaldehyde

https://huagongshe.com/reaction/412166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Benzyloxy)-5-hydroxybenzaldehydeHCID 18536192—
SolventDimethylformamideHCID 6228—
Product2-Benzyloxy-5-[(2-propenyl)oxy]benzaldehydeHCID 18536183—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of the product from Step A (75.4 mmol) in 100 mL of DMF was added potassium carbonate (20.8 g, 150.7 mmol), followed by allyl bromide (11.7 mL, 135 mmol). The reaction was warmed to 60° C. and stirred for one hour. The solution was poured into EtOAc and washed with water, saturated NaHCO3 solution and brine, dried (Na2SO4), filtered, and concentrated in vacuo. The resulting product was purified by silica gel chromatography (20-30% EtOAc/hexane) to provide the titled product, along with unreacted starting material (4.39 g, 26%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562823B1
Source datasetuspto-grants-2003_05
ORD IDord-1b40a4cf657d453cb3e06a20ba23ab57
Source noteuspto-grants-2003_05