Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004626Generated: October 25, 2026

Allyl iodide → 3-(2-Ethylphenyl)-1-propene

https://huagongshe.com/reaction/1004626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl iodideHCID 11166—
Reactant1-Bromo-2-ethylbenzeneHCID 16089—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Ethylphenyl)-1-propeneHCID 18694504—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a suspension of 8.53 g (350 mmol) of magnesium in 270 mL of dry THF was added 50 g (270 mmol) of 1-bromo-2-ethyl benzene. The temperature was maintained at 50° C. during addition, then was heated under reflux. After 1 h, the solution was cooled to -78° C. under N2, and 54.42 g (324 mmol) of allyl iodide was added dropwise. The mixture was allowed to warm to room temperature, stirred for an additional 2 h, then cooled to 0° C. The reaction was quenched by addition of 2M HCl and 500 mL of ether and the layers were separated. The organic layer was washed with 30 mL of saturated NaHCO3 solution and brine, dried over MgSO4, filtered and concentrated. The oily residue was filtered through silica gel with 20% ethyl acetate-hexane and the eluate was concentrated to afford the crude 1-allyl-2-ethylbenzene as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051590
Source datasetuspto-grants-2000_04
ORD IDord-5fc41e887c3041568b2ae8708bc7e2d7
Source noteuspto-grants-2000_04