HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236886Generated: November 2, 2026
Potassium Carbonate → 1-(3-Furanyl)-4-methyl-2(1H)-pyridinone
https://huagongshe.com/reaction/2236886
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromofuran | HCID 89164 | — |
| Reactant | HCID 178428601 | HCID 178428601 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | 1-(3-Furanyl)-4-methyl-2(1H)-pyridinone | HCID 42625744 | 62% |
Reaction Steps
A mixture of 2-hydroxy-4-methylpyridine (0.66 g, 6.0 mmol), 3-bromofuran (1.7 g, 12 mmol), copper (I) iodide (0.11 g, 0.60 mmol), and potassium carbonate (0.84 g, 6.0 mmol) in N,N-dimethylformamide (12 mL) were heated at 180° C. for 2 hours in a 300 W microwave reactor. The completed reaction mixture is diluted with 10% aqueous ammonium hydroxide solution and extracted 3× with ethyl acetate. The combined extracts were washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give 1-furan-3-yl-4-methyl-1H-pyridin-2-one (0.65 g, 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713994B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-51cffdd047504f8388a7dd64227ac683 |
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| Source note | uspto-grants-2010_05 |
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