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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 458567Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/458567

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktIsatoic AnhydrideHCID 8359—
EduktSodium hydrideHCID 24758—
EduktDimethylacetamideHCID 31374—
Edukt2,2-DiethylpropanedioateHCID 6951563—
EduktHCID 178418361HCID 178418361—
ProduktEthyl 4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylateHCID 5468445847%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07192955B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-ec9b032688a047559d153e8360dcba5a
Quellennotizuspto-grants-2007_03