Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | HCID 178471925 | HCID 178471925 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 3245723 | HCID 3245723 | 99% |
Reaction Steps
Diphenyl ether (150 ml, 943 mmol) was heated to boiling and ethyl 4-((2-(ethoxycarbonyl)-3-oxobut-1-en-1-yl)amino)benzoate (6.84 g, 22.40 mmol) was added slowly. After the addition, the reaction was allowed to stir at 200-250° C. for another 30 min. After cooling, the reaction was diluted with hexane, filtered, and the precipitate was washed with hexane/diethyl ether, collected and dried to give ethyl 3-acetyl-4-oxo-1,4-dihydroquinoline-6-carboxylate (5.74 g, 22.14 mmol, 99% yield) as tan solid. LCMS: (M+H)+: 260.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340556B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-8be532b4d75746018f9a903ff41b2bec |
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| Source note | uspto-grants-2016_05 |
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