HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen → 6-Ethyl-4-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Cyanoacetamide | HCID 7898 | — |
| Reactant | 3-Hexen-2-one | HCID 5367744 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 6-Ethyl-4-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile | HCID 10630830 | 21% |
Reaction Steps
To a solution of t-BuOK (17.2 g, 153 mmol) and cyanoacetamide (13 g, 153 mmol) in CH3CN (225 mL) was added (3E)-3-hexen-2-one (15 g, 153 mmol) at room temperature under N2 atmosphere. The reaction mixture was stirred for 30 min. To the reaction mixture was added additional t-BuOK (51.4 g), and the N2 was displaced by oxygen. After stirring for 1 h without external cooling, the mixture was diluted with 4 N HCl, which was added slowly and with good stirring. The mixture was filtered, washed with EtOH, dried to give 6-ethyl-4-methyl-2-oxo-1,2-dihydro-3-pyridinecarbonitrile (5 g, 21%). 1H NMR (400 MHz, DMSO-d6) δ 12.33 (br. s., 1H), 6.18 (s, 1H), 2.45 (q, 2H), 2.30 (s, 3H), 1.11 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09446041B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-f41343517eb64ef685fbc315d69685c5 |
| Source note | uspto-grants-2016_09 |