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
Participants
| Role | Name | HCID | Charge |
|---|
| 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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03985882 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-9af346842f51492db9cfb014ec756086 |
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| Source note | uspto-grants-1976_10 |
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