HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3-Nitrobenzaldehyde → 3-Acetyl-2-methyl-4-(3-nitrophenyl)-4,6,7,8-tetrahydro-5(1H)-quinolone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Edukt | 1,3-Cyclohexanedione | HCID 10434 | — |
| Edukt | 4-Amino-3-penten-2-one | HCID 136873 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 3-Acetyl-2-methyl-4-(3-nitrophenyl)-4,6,7,8-tetrahydro-5(1H)-quinolone | HCID 14955186 | 40,2% |
Reaktionsschritte
4-Amino-3-penten-2-one (2.00 g), 1,3-cyclohexanedione (2.30 g), and 3-nitrobenzaldehyde (3.08 g) were combined in ethanol (180 mL) and heated at reflux for 5 hours. A yellow solid formed upon cooling to ambient temperature. The solid was purified by trituration with hot ethyl acetate/ethanol to yield the title compound (2.65 g) as a yellow solid; mp >250° C.; NMR: 1.67-1.97 (m,2, CH2), 2.13 (s,3, CH3), 2.22 (m,2, CH2), 2.35 (s,3, CH3), 2.47 (m,2, CH2), 5.11 (s,1, CH), 7.52 (m, 1, Ar), 7.60 (d,1, J=7.7, Ar), 7.97 (m,2, Ar), 9.32 (s,1, NH); MS: m/z=326(M). Analysis for C18H18N2O4 : Calculated: C, 66.25; H, 5.56; N, 8.58, Found: C, 65.99; H, 5.61; N, 8.40.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05622964 |
| Quelldatensatz | uspto-grants-1997_04 |
| ORD ID | ord-a98e258a9bb24f818da0d7393421658b |
| Quellennotiz | uspto-grants-1997_04 |