HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4,6-Dimethyl-3-nitropyridin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetylacetone | HCID 31261 | — |
| Reactant | Ethyl nitroacetate | HCID 69379 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | 4,6-Dimethyl-3-nitropyridin-2(1H)-one | HCID 535972 | 104.1% |
Reaction Steps
A mixture of ethyl nitroacetate (80.0 g, 601 mmol) in ammonium hydroxide (25% NH3 in water, 400 mL) was stirred at room temperature for 3 days, and then the solution was concentrated by air-drying. The residue was dissolved in water (450 mL). To the solution was added 2,4-pentanedione (73.1 g, 730 mmol), pyridine (16.2 mL, 200 mmol) and acetic acid (11.4 mL, 200 mmol), and the mixture was stirred for an additional 7 days. The resulting precipitates were collected by filtration and dried under reduced pressure to give 35.0 g (35%) of the title compound as yellow solids: 1H-NMR (DMSO-d6) δ 12.44 (1H, br.s), 6.06 (1H, s), 2.19 (3H, s), 2.13 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07928119B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-68dd7996428640c6b31d4f6d7114319f |
| Source note | uspto-grants-2011_04 |