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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 346643Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/346643

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDiethyl MalonateHCID 7761—
EduktIsatoic AnhydrideHCID 8359—
EduktSodium hydrideHCID 24758—
EduktHCID 178418361HCID 178418361—
LösungsmittelDimethylacetamideHCID 31374—
ProduktEthyl 4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylateHCID 5468445833,1%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

Neat diethyl malonate (18.05 g, 112.7 mmol) was added slowly to a suspension of sodium hydride (60% in mineral oil, 4.96 mg, 124 mmol) in dimethylacetamide under N2 atmosphere. The mixture was stirred at room temperature until the evolution of hydrogen gas ceased, then the mixture was heated to 90° C. for 30 min. and cooled to room temperature. A solution of isatoic anhydride (20 g, 124 mmol) in dimethylacetamide was added slowly and the mixture heated overnight at 110° C. 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 8.7 g (30%) of white solids. M.P. 173° C. 1H NMR (DMSO-d6): δ 1.31 (t, J=6.6 Hz, 3H), 4.34 (q, J=6.6 Hz, 2H), 7.20 (t, J=8.0 Hz, 1H), 7.27 (d, J=8.4 Hz, 1H), 7.62 (t, J=7.2 Hz, 1H), 7.93 (d, J=8.0 Hz, 1H), 11.50 (b, 1H); EIMS: 234 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07173036B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-b8ea3996c6ec4d80ae73da7d15e199b6
Quellennotizuspto-grants-2007_02