Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | O-Toluidine | HCID 7242 | — |
| Reactant | 2-Hydroxy-1-naphthaldehyde | HCID 12819 | — |
| Product | HCID 68154097 | HCID 68154097 | — |
Reaction Steps
3.44 g (20.0 mmol) of 2-hydroxy-1-naphthaldehyde was dissolved in 50 ml ethanol under heating, and 2.14 g (20.0 mmol) of o-toluidine 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-methylaniline (hereinafter, also referred to as “HNOT”) as a yellow crystal (4.24 g, 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08715523B2 |
|---|
| Source dataset | uspto-grants-2014_05 |
|---|
| ORD ID | ord-390cbfb13a4b4ad39385d9afed975b43 |
|---|
| Source note | uspto-grants-2014_05 |
|---|