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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228811Generated: October 25, 2026

Hydrochloric Acid → (4,5-Dimethylfuran-2-yl)-(2-pyridyl)-methanone

https://huagongshe.com/reaction/228811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantPyridine-2-carbonitrileHCID 7522—
Reactant2,3-DimethylfuranHCID 34337—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
Product(4,5-Dimethylfuran-2-yl)-(2-pyridyl)-methanoneHCID 2307848417%

Reaction Conditions

Temperature0 °C

Reaction Steps

2,3-Dimethylfuran (5 g) was dissolved in diethyl ether (75 ml) under an argon atmosphere. A 1.6 M hexane solution (35.7 ml) of n-butyllithium was added dropwise thereto at 0° C., and the mixture was stirred under reflux for 2.5 hr. Thereafter, the reaction solution was cooled to −78° C., a solution of 2-cyanopyridine (6.0 g) in diethyl ether (20 ml) was added dropwise thereto, and the mixture was stirred at room temperature for 3 hr. The reaction solution was poured into ice to stop the reaction. The reaction solution was adjusted to pH 5 by the addition of 2 M hydrochloric acid and was then extracted with chloroform. The chloroform layer was then washed with water and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography using hexane-ethyl acetate to give (4,5-dimethylfuran-2-yl)-(2-pyridyl)-methanone (1.8 g, yield 17%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-4709ba83186d4c28af7547d3e5d405a5
Source noteuspto-grants-2009_07