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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445562Generated: October 31, 2026

Imidazole → HCID 86612631, compound

https://huagongshe.com/reaction/1445562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant2-Cyclohexen-1-oneHCID 13594—
Reactant2-Chloro-5-(4-methoxyphenyl)pyridine-3-carbaldehydeHCID 15459226—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 86612631HCID 8661263191%

Reaction Steps

The clear solution of 2-Chloro-5-(4-methoxyphenyl)-nicotinaldehyde (10 mmol, 2.45 g) and imidazole (10 mmol) in 50 ml. of MeOH was slowly charged with 50 ml. of deionized water. To a stirred homogeneous reaction mixture was added 2-cyclohexen-1-one (10.2 mmol., 1.0 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 91% yield (3.13 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666883B2
Source datasetuspto-grants-2010_02
ORD IDord-b96204621b934505ab25d25350c51f79
Source noteuspto-grants-2010_02