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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 14355Erstellt: 23. Oktober 2026

Hydrochloric Acid → 4-Hydroxy-1-methyl-3-nitro-1,2-dihydroquinolin-2-one

https://huagongshe.com/de/reaction/14355

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium hydrideHCID 24758—
EduktN-Methylisatoic anhydrideHCID 25160—
EduktEthyl nitroacetateHCID 69379—
EduktHCID 178418361HCID 178418361—
LösungsmittelDimethylacetamideHCID 31374—
Produkt4-Hydroxy-1-methyl-3-nitro-1,2-dihydroquinolin-2-oneHCID 5468212327%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A solution of ethylnitroacetate (15.96 g, 120 mmol) was added slowly in a suspension of sodium hydride (60% in mineral oil, 5.28 g, 132 mmol) 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 N-methylisatoic anhydride (23.38 g, 132 mmol) in dimethylacetamide was added slowly and heated overnight at 120° 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 7.1 g (27%) of yellow solids. Mp 193° C. 1H NMR (DMSO-d6): δ 3.60 (s, 3H), 7.37 (t, J=7.6 Hz, 1H), 7.58 (d, J=8.5 Hz, 1H), 7.77 (t, J=7.5 Hz, 1H), 8.12 (d, J=7.9 Hz, 1H). EIMS m/z 221 (M+1), 243 (M+23). Anal. (C10H8N2O4) C, H, N.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732146B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-f5f4df6862dd4fd2a27a8204c0be1017
Quellennotizuspto-grants-2010_06