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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267456Generated: November 2, 2026

Allyl bromide → Methyl 4-(3-bromopropyl)benzoate

https://huagongshe.com/reaction/1267456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantMethyl 4-(3-hydroxypropyl)benzoateHCID 14425137—
SolventAcetonitrileHCID 6342—
ProductMethyl 4-(3-bromopropyl)benzoateHCID 10801120—

Reaction Steps

A solution of 4-(3-hydroxy-propyl)-benzoic acid methyl ester (11.98 g) and 1,1′-carbonyldiimidazole (9.0 g, 55.50 mmol) in CH3CN (200 mL) was stirred at room temperature for 1.5 h. Allyl bromide (20 mL) was added and the reaction mixture was heated under reflux for 20 h. The reaction mixture was cooled to room temperature and saturated aqueous NaHCO3was added. The aqueous solution was washed with EtOAc (3×) and the organic solutions were combined, dried (MgSO4), filtered and concentrated. Purification by medium pressure chromatography (9:1 hexanes:EtOAc) provided the title compound of Preparation 4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552067B2
Source datasetuspto-grants-2003_04
ORD IDord-de73f29a3217447d97d9c0e53e0722b2
Source noteuspto-grants-2003_04