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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287876Generated: October 31, 2026

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

https://huagongshe.com/reaction/1287876

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 3 hours. Polyphosphoric acid (200 g.) is as added, and the mixture is heated gradually to 220° C. then maintained at 220° c. for 1 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 numberUS03985882
Source datasetuspto-grants-1976_10
ORD IDord-9af346842f51492db9cfb014ec756086
Source noteuspto-grants-1976_10