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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37822Generated: October 26, 2026

2-Methylpyridine → 1-(2-Cyclopent-1-enyl-2-oxo-ethyl)-2-methyl-pyridinium bromide salt

https://huagongshe.com/reaction/37822

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylpyridineHCID 7975—
Reactant2-Bromo-1-(1-bromo-cyclopentyl)-ethanoneHCID 12466593—
SolventAcetoneHCID 180—
Product1-(2-Cyclopent-1-enyl-2-oxo-ethyl)-2-methyl-pyridinium bromide saltHCID 86639594117.6%

Reaction Steps

2-Bromo-1-(1-bromo-cyclopentyl)-ethanone (3.7 g, 13.7 mmol) and α-picoline (1.02 g, 11.0 mmol) in acetone were heated at reflux overnight. The reaction mixture was allowed to cool then concentrated in vacuo. The crude mass was washed with 30% ethyl acetate/petroleum ether and diethyl ether. 1-(2-Cyclopent-1-enyl-2-oxo-ethyl)-2-methyl-pyridinium bromide salt (3.65 g, 94%) was obtained as a semi-solid material and taken for next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524705B2
Source datasetuspto-grants-2013_09
ORD IDord-c29a18fee9b8430f971d96da9a294c69
Source noteuspto-grants-2013_09