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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298152Generated: October 29, 2026

Allyl bromide → 1-(3-Bromopropyl)-3-chlorobenzene

https://huagongshe.com/reaction/2298152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantEthyl AcetateHCID 8857—
Reactant3-(3-Chlorophenyl)propan-1-olHCID 9989667—
SolventAcetonitrileHCID 6342—
SolventSodium chloride; waterHCID 57417360—
Product1-(3-Bromopropyl)-3-chlorobenzeneHCID 1408486085%

Reaction Steps

A solution of 3-(3-chloro-phenyl)-propan-1-ol (12.54 g, 73.6 mmol) and N,N′-carbonyl diimidazole (13.12 g, 81 mmol) in CH3CN was stirred at room temperature for 1 h. Allyl bromide (53.43 g, 442 mmol) was added and the reaction was heated at reflux for 24 h. The reaction was cooled to room temperature and brine and EtOAc were added. The aqueous solution was extracted with EtOAc and the organic solution was dried (MgSO4), filtered, and concentrated. Flash chromatography provided the title compound in about 85% yield. 1H NMR (400 MHz, CDCl3) δ 7.30-7.09 (m, 4H), 3.38 (t, 2H), 2.76 (t, 2H), 2.15 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492412B2
Source datasetuspto-grants-2002_12
ORD IDord-0b4448bdf54c41e9847d1c790d70e5b5
Source noteuspto-grants-2002_12