Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-Aminobenzaldehyde | HCID 68255 | — |
| Reactant | Ethyl nitroacetate | HCID 69379 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2(1H)-Quinolinone, 3-nitro- | HCID 9990061 | 51% |
Reaction Steps
2-Aminobenzaldehyde (1.75 g, 14.5 mmol) was dissolved in xylene (87.5 mL). To this, ethyl 2-nitroacetate (6.43 mL, 58.0 mmol) and piperidine (1.58 mL, 16.0 mmol) were added and the mixture was stirred with heat at 150° C. for 1.5 hours and successively stirred with cooling in an ice bath for 0.5 hour. The precipitate was collected by filtration and dried under reduced pressure. Thus, 3-nitroquinolin-2(1H)-one (1.40 g, yield: 51%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673908B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-8ca3d927426e48d1abcf9e1245058ea7 |
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| Source note | uspto-grants-2014_03 |
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