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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890744Generated: October 29, 2026

Triphenylphosphine → 4-Vinylbenzyl bromide

https://huagongshe.com/reaction/890744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
Reactant(4-Vinylphenyl)methanolHCID 2735162—
SolventDichloromethaneHCID 6344—
Product4-Vinylbenzyl bromideHCID 64026933.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

Bromine (16.4 g, 103 mmol) was slowly added to a solution of triphenylphosphine (28.87 g, 110.1 mmol) in CH2Cl2 (260 mL) at 0° C. After 10 minutes, 4-vinylbenzyl alcohol (12.5 g, 93.3 mmol) was added and the reaction mixture was stirred at 0° C. for 2 h. The reaction mixture was washed with water (1×) followed by brine (1×). The organic solution was dried over MgSO4, filtered, and concentrated in vacuo. The product was triturated with petroleum ether (3×), and the ethereal solution was concentrated in vacuo. The residue was purified by flash chromatography (hexanes) to afford 4-vinyl-benzyl bromide (6.23 g). 1H NMR (400 MHz, CDCl3) δ 7.32–7.45 (m, 4H), 6.72 (dd, 1H), 5.77 (d, 1H), 5.28 (d, 1H), 4.50 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06998423B2
Source datasetuspto-grants-2006_02
ORD IDord-2cbeeb0a1a0b4a35a2f6c88d3615d1e7
Source noteuspto-grants-2006_02