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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836689Generated: November 1, 2026

2-Bromobenzyl bromide → 2-(But-3-en-1-yl)bromobenzene

https://huagongshe.com/reaction/1836689

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromobenzyl bromideHCID 76965—
ReactantHCID 178455850HCID 178455850—
SolventTetrahydrofuranHCID 8028—
Product2-(But-3-en-1-yl)bromobenzeneHCID 3485712—

Reaction Steps

To an ice cold solution of 2-bromobenzyl bromide (5.00 g, 0.020 mol) in THF (25 mL) was added 1M allyl magnesium bromide (100 mL, 0.100 mol) slowly via cannula. The reaction mixture was stirred at reflux for 1.5 h, cooled in an ice bath and quenched with 50 mL of aqueous 2M H2SO4. Water (50 mL) was added to dissolve any remaining solid and the layers were separated. The aqueous layer was extracted with Et2O (2×150 mL). The combined organic extracts were dried over Na2SO4, filtered and concentrated to yield 1-bromo-2-but-3-enyl-benzene as a light yellow oil. The isolated crude product was carried forward without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777421B2
Source datasetuspto-grants-2004_08
ORD IDord-8b9f36c2c6734251a543a45e99dc576f
Source noteuspto-grants-2004_08