HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414315Generated: November 4, 2026
Methane → 6,7-dihydro-9-methoxy-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid
https://huagongshe.com/reaction/1414315
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methane | HCID 297 | — |
| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Quinoline, 1,2,3,4-tetrahydro-6-methoxy- | HCID 67113 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6,7-dihydro-9-methoxy-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid | HCID 13094360 | — |
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 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 2 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04001243 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-851b0fd8d1c34ea6a43d18247395f70d |
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| Source note | uspto-grants-1977_01 |
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