Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cuminaldehyde | HCID 326 | — |
| Reactant | 2-Hydrazinopyridine | HCID 78645 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 70208316 | HCID 70208316 | 76% |
Reaction Steps
In 20 ml of ethanol was dissolved 5.46 g of 2-hydrazinopyridine. With 7.41 g of 4-isopropylbenzaldehyde added, the solution was agitated. Fine crystals started precipitating within about 30 seconds and the entire solution solidified within about 1 minute. 10 ml of ethanol was added to the mass, which was refluxed at 100° C. for 40 minutes. 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 ethanol and dried in vacuum for 40 minutes, obtaining 9.09 g (yield 76%) of pale 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-d826a2186de74cd1a59c742bd16cfaa7 |
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| Source note | uspto-grants-1997_02 |
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