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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921207Generated: October 31, 2026

3-Bromobenzyl bromide → 1-Bromo-3-(but-3-en-1-yl)benzene

https://huagongshe.com/reaction/921207

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromobenzyl bromideHCID 69979—
ReactantHCID 178455850HCID 178455850—
SolventTetrahydrofuranHCID 8028—
Product1-Bromo-3-(but-3-en-1-yl)benzeneHCID 1572516583%

Reaction Steps

A mixture of 1-bromo-3-(bromomethyl)benzene (1 g, 4.00 mmol) in THF (15 mL) was added allylmagnesium bromide (4.80 mL, 4.80 mmol) and stirred at rt for 1 h, then refluxed for 2 h. It was then quenched with NH4Cl, extracted with EtOAc. The organic layer was dried over MgSO4, filtered and concentrated to obtain an oil. It was then purified by 5% EtOAc/hexane to isolate 1-bromo-3-(but-3-en-1-yl)benzene (0.7 g, 3.32 mmol, 83% yield) as an oil. 1H NMR (400 MHz, CDCl3) δ 7.41-7.31 (m, 2H), 7.21-7.12 (m, 2H), 5.85 (ddt, J=17.1, 10.3, 6.6 Hz, 1H), 5.14-4.94 (m, 2H), 2.75-2.64 (m, 2H), 2.45-2.31 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273067B2
Source datasetuspto-grants-2016_03
ORD IDord-e1b2300de3c445f3b3b0e10b03029053
Source noteuspto-grants-2016_03