Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Aminobiphenyl | HCID 7015 | — |
| Reactant | 2-Hydroxy-1-naphthaldehyde | HCID 12819 | — |
| Product | HCID 68154273 | HCID 68154273 | — |
Reaction Steps
3.44 g (20.0 mmol) of 2-hydroxy-1-naphthaldehyde was dissolved in 50 ml ethanol under heating, and 3.38 g (20.0 mmol) of 2-aminobiphenyl was added. After stirring under reflux at 70° C. for 1 hour, completion of the reaction was confirmed by TLC. The solution was concentrated with an evaporator to about 30 ml, whereupon a crystal was formed, which was filtered by Kiriyama funnel. Drying under reduced pressure at 25° C. for 24 hours gave 2-hydroxy-1-naphthylmethylidene-2-phenylaniline (hereinafter, also referred to as “HNBP”) as a yellow crystal (5.62 g, 87%).
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-6486b7daf90b442b849432b60090f747 |
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| Source note | uspto-grants-2014_05 |
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