Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6692Generated: October 26, 2026

Hydrochloric Acid → Ethyl 4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylate

https://huagongshe.com/reaction/6692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsatoic AnhydrideHCID 8359—
ReactantSodium hydrideHCID 24758—
ReactantDimethylacetamideHCID 31374—
Reactant2,2-DiethylpropanedioateHCID 6951563—
ReactantHCID 178418361HCID 178418361—
ProductEthyl 4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylateHCID 5468445847%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of diethylmalonate (80 g, 0.50 mol) was added slowly to a suspension of sodium hydride (60% in mineral oil, 22 g, 0.55 mol) 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 isatoic anhydride (89.72 g, 0.55 mmol) in dimethylacetamide was added slowly and heated at 120° C. for 15 h. 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 55 g (47%) of white solids. Mp 173° C. 1H NMR (DMSO-d6): δ 1.30 (t, J=6.9 Hz, 3H), 4.33 (q, J=6.9 Hz, 2H), 7.18 (t, J=7.5 Hz, 1H), 7.26 (d, J=8.2 Hz, 1H), 7.62 (t, J=7.2 Hz, 1H), 7.93 (d, J=8.0 Hz, 1H) 11.50 (s, 1H), 13.5 (s, 1H). EIMS m/z 234 (M+1), 256 (M+23). Anal. (C12H11NO4) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084141B2
Source datasetuspto-grants-2006_08
ORD IDord-5e984f0bb90a49f49c73a342593a21ea
Source noteuspto-grants-2006_08