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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219710Generated: November 1, 2026

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

https://huagongshe.com/reaction/2219710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantSodium BicarbonateHCID 516892—
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 NaHCO3 was 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 numberUS07414071B2
Source datasetuspto-grants-2008_08
ORD IDord-4b2025e0318b410fb628658a51b4c732
Source noteuspto-grants-2008_08