HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitrobenzaldehyde → 3-Acetyl-2-methyl-4-(3-nitrophenyl)-4,6,7,8-tetrahydro-5(1H)-quinolone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | 1,3-Cyclohexanedione | HCID 10434 | — |
| Reactant | 4-Amino-3-penten-2-one | HCID 136873 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Acetyl-2-methyl-4-(3-nitrophenyl)-4,6,7,8-tetrahydro-5(1H)-quinolone | HCID 14955186 | 40.2% |
Reaction Steps
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 .
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05455253 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-4bc3e67b498840d0a5bb015f0b5196e6 |
| Source note | uspto-grants-1995_10 |