Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cuminaldehyde | HCID 326 | — |
| Reactant | 2-Hydrazinyl-5-nitropyridine | HCID 4031931 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 95915 | HCID 95915 | 62.8% |
Reaction Steps
In 50 ml of ethanol were dispersed 3.03 g of 2-hydrazino-5-nitropyridine and 3.08 g of 4-isopropylbenzaldehyde. The dispersion was refluxed at 90° C. for one hour. The reaction solution was allowed to cool at room temperature and further cooled down to 5° to 10° C. to cause crystals to fully precipitate, which were collected by suction filtration. The crystals were washed with a small amount of ethanol and dried in vacuum at 60° C. for 1.5 hours, obtaining 3.51 g (yield 62%) of dark yellow acicular crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05604004 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-784717d5fd5b42a4bdb90b355e72cca0 |
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| Source note | uspto-grants-1997_02 |
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