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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597521Generated: October 25, 2026

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

https://huagongshe.com/reaction/597521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
ReactantSodium HydroxideHCID 14798—
ReactantQuinoline, 1,2,3,4-tetrahydro-6-methoxy-HCID 67113—
SolventWaterHCID 962—
Product6,7-dihydro-9-methoxy-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acidHCID 13094360—

Reaction Conditions

Temperature220 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04014877
Source datasetuspto-grants-1977_03
ORD IDord-0e66ceb581544733b3ae21efff3a4b0e
Source noteuspto-grants-1977_03