HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 14355Erstellt: 23. Oktober 2026
Hydrochloric Acid → 4-Hydroxy-1-methyl-3-nitro-1,2-dihydroquinolin-2-one
https://huagongshe.com/de/reaction/14355
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | N-Methylisatoic anhydride | HCID 25160 | — |
| Edukt | Ethyl nitroacetate | HCID 69379 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 4-Hydroxy-1-methyl-3-nitro-1,2-dihydroquinolin-2-one | HCID 54682123 | 27% |
Reaktionsschritte
A solution of ethylnitroacetate (15.96 g, 120 mmol) was added slowly in a suspension of sodium hydride (60% in mineral oil, 5.28 g, 132 mmol) in dimethylacetamide under N2 atmosphere. The mixture was allowed to stir at room temperature until the evolution of hydrogen gas ceased, then heated to 90° C. for 30 min. and cooled to room temperature. A solution of N-methylisatoic anhydride (23.38 g, 132 mmol) in dimethylacetamide was added slowly and heated overnight at 120° C. The mixture was cooled to room temperature, poured into ice water, and acidified by cold 10% HCl. The solids formed were filtered and washed several times by water to yield 7.1 g (27%) of yellow solids. Mp 193° C. 1H NMR (DMSO-d6): δ 3.60 (s, 3H), 7.37 (t, J=7.6 Hz, 1H), 7.58 (d, J=8.5 Hz, 1H), 7.77 (t, J=7.5 Hz, 1H), 8.12 (d, J=7.9 Hz, 1H). EIMS m/z 221 (M+1), 243 (M+23). Anal. (C10H8N2O4) C, H, N.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07732146B2 |
|---|
| Quelldatensatz | uspto-grants-2010_06 |
|---|
| ORD ID | ord-f5f4df6862dd4fd2a27a8204c0be1017 |
|---|
| Quellennotiz | uspto-grants-2010_06 |
|---|