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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380125Generated: November 1, 2026

Allyl bromide → (Pent-4-en-1-yl)benzene

https://huagongshe.com/reaction/1380125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantHCID 178419670HCID 178419670—
SolventTetrahydrofuranHCID 8028—
Product(Pent-4-en-1-yl)benzeneHCID 517892—

Reaction Steps

A solution of phenethyl magnesium bromide (prepared from 25 l g, 0.135 mol of phenethyl bromide and excess magnesium turnings) in anhydrous tetrahydrofuran (50 ml) was added to a stirred solution of allyl bromide (16.34 g, 0.135 mol) in anhydrous tetrahydrofuran (150 ml) at room temperature and under an atmosphere of dry nitrogen. The mixture was stirred at room temperature for 3 hours and the solvent was then evaporated off under reduced pressure and the residue was dissolved in ethyl acetate. The solution was washed with a saturated aqueous solution of ammonium chloride and the solvent was evaporated off under reduced pressure to give an oil which was distilled to give 5-phenylpent-1-ene as a colourless oil (b.p. 40° C., 0.5 mm, Hg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04579862
Source datasetuspto-grants-1986_04
ORD IDord-f8358a5990264efc818245dcb3d19efe
Source noteuspto-grants-1986_04