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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445553Generated: October 26, 2026

Imidazole → 2-[(2-Chloro-5-ethyl pyridine-3-yl)(hydroxy)methyl]cyclopent-2-en-1-one

https://huagongshe.com/reaction/1445553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant2-Cyclopenten-1-oneHCID 13588—
Reactant2-Chloro-5-ethylpyridine-3-carbaldehydeHCID 24976845—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-[(2-Chloro-5-ethyl pyridine-3-yl)(hydroxy)methyl]cyclopent-2-en-1-oneHCID 5888023997%

Reaction Steps

The clear solution of 2-Chloro-5-ethylnicotinaldehyde (10 mmol, 1.69) and imidazole (10 mmol, 0.68 g) in 50 ml. of MeOH was slowly charged with 50 ml. of deionized water. To a stirred homogeneous reaction mixture was added 2-cyclopenten-1-one (10.2 mmol., 0.88 g) at room temperature and reaction progress was monitored by TLC. Upon completion of the reaction, excess MeOH was removed under reduced pressure, washed with water and extracted with CHCl3 thrice. Combined organic layers were washed with brine solution twice. The organic layer was concentrated and column chromatography of the crude product on silica gel, using 30% EtOAC in hexane as eluent, gave pure Baylis-Hillman adduct in 97% yield (2.47 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666883B2
Source datasetuspto-grants-2010_02
ORD IDord-a26340e2a3c941729c95c0fdf97fa665
Source noteuspto-grants-2010_02