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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58873Generated: October 26, 2026

Benzyl Bromide → Benzyl cyclopent-3-enecarboxylate

https://huagongshe.com/reaction/58873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Cyclopentene-1-carboxylic acidHCID 853756—
SolventAcetonitrileHCID 6342—
ProductBenzyl cyclopent-3-enecarboxylateHCID 2208426174%

Reaction Steps

K2CO3 (35.0 g, 255 mmol) was added to a solution of cyclopent-3-enecarboxylic acid (20.0 g, 178 mmol) in acetonitrile (500 mL) followed by addition of benzyl bromide (36.6 g, 214 mmol). The reaction mixture was stirred for 12 h at ambient temperature. The mixture was filtered and washed with acetonitrile (200 mL). The filtrate and washings were combined and concentrated to dryness. The residue was purified by flash column chromatography on silica gel (hexane/EtOAc=10:1) to afford benzyl cyclopent-3-enecarboxylate (26.5 g, 74% yield) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434761B2
Source datasetuspto-grants-2016_09
ORD IDord-34cebf29e9254682a414ec0d9d3bf15b
Source noteuspto-grants-2016_09