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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209528Generated: October 25, 2026

3-Nitrobenzaldehyde → 3-Acetyl-2-methyl-4-(3-nitrophenyl)-4,6,7,8-tetrahydro-5(1H)-quinolone

https://huagongshe.com/reaction/2209528

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrobenzaldehydeHCID 7449—
Reactant1,3-CyclohexanedioneHCID 10434—
Reactant4-Amino-3-penten-2-oneHCID 136873—
SolventEthanolHCID 702—
Product3-Acetyl-2-methyl-4-(3-nitrophenyl)-4,6,7,8-tetrahydro-5(1H)-quinoloneHCID 1495518640.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455253
Source datasetuspto-grants-1995_10
ORD IDord-4bc3e67b498840d0a5bb015f0b5196e6
Source noteuspto-grants-1995_10