Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylquinoline | HCID 7060 | — |
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7251-91-4 | HCID 5376617 | 88% |
Reaction Steps
To 3.1 g of acetic anhydride, 7.2 g of quinaldine and 7.6 g of m-nitrobenzaldehyde were added and the resulting mixture was stirred under nitrogen atmosphere at 160° C. for 4 hours. After completion of the reaction, water was added to the reaction mixture and the resulting solid was collected by filtration and dried. Recrystallization from toluene gave 12.1 g (yield: 88%) of the captioned compound as an yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04749701 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-6805216384184842b8c78adcbe30a236 |
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| Source note | uspto-grants-1988_06 |
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