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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Pyridine-2-carbonitrile | HCID 7522 | — |
| Reactant | 2,3-Dimethylfuran | HCID 34337 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (4,5-Dimethylfuran-2-yl)-(2-pyridyl)-methanone | HCID 23078484 | 17% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560558B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-4709ba83186d4c28af7547d3e5d405a5 |
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| Source note | uspto-grants-2009_07 |
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