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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 597521Erstellt: 24. Oktober 2026

Methane → 6,7-dihydro-9-methoxy-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid

https://huagongshe.com/de/reaction/597521

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethaneHCID 297—
EduktDiethyl (ethoxymethylene)malonateHCID 6871—
EduktSodium HydroxideHCID 14798—
EduktQuinoline, 1,2,3,4-tetrahydro-6-methoxy-HCID 67113—
LösungsmittelWaterHCID 962—
Produkt6,7-dihydro-9-methoxy-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acidHCID 13094360—

Reaktionsbedingungen

Temperatur220 °C

Reaktionsschritte

Diethyl ethoxymethylenemalonate (43.2 g., 0.20 mole) and 6-methoxytetrahydroquinoline (32.6 g., 0.20 mole) are mixed and heated at 125°-130° C. for three hours. Polyphosphoric acid (200 g.) is added, and the mixture is heated gradually to 220° C. then maintained at 220° C. for one hour. The mixture containing the product ester of Formula III is poured into about 600 ml. of water, then made basic with 40 percent sodium hydroxide solution and heated on a steam bath for two hours. The solution is treated with decolorizing charcoal, filtered and acidified. The solid product is isolated by filtration, washed with water and ethanol, then recrystallized from N,N-dimethylformamide to give 6,7-dihydro-9-methoxy-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid, m.p. 253°-257° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04014877
Quelldatensatzuspto-grants-1977_03
ORD IDord-0e66ceb581544733b3ae21efff3a4b0e
Quellennotizuspto-grants-1977_03