Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 2-Hydroxy-1-naphthaldehyde | HCID 12819 | — |
| Product | HCID 11075772 | HCID 11075772 | — |
Reaction Steps
6.88 g (40.0 mmol) of 2-hydroxy-1-naphthaldehyde was dissolved in 10 ml ethanol under heating, and 3.72 g (40.00 mmol) of aniline was added. After stirring under reflux at 70° C. for 1 hour, completion of the reaction was confirmed by TLC. Upon being left at rest over night in the refrigerator, a crystal was formed, and the resulting precipitation was filtered by Kiriyama funnel. Drying under reduced pressure at 25° C. for 24 hours gave 2-hydroxy-1-naphthylmethylidene aniline (hereinafter, also referred to as “HNA”) as a yellow crystal (9.17 g, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08715523B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-d36ce22a7706466c850f10806f51a16c |
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| Source note | uspto-grants-2014_05 |
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