Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | 2-Naphthol | HCID 8663 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 14676218 | HCID 14676218 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 135718525 | HCID 135718525 | — |
Reaction Steps
Next, a flask was loaded with sodium ethylate (1.6 g), ethanol (14 ml), and 2-amino-3-propoxypyridine (3.8 g), and they were mixed. To the mixture, isopentyl nitrite (2.7 g) was dropwise added in 20 minutes with stirring. This was stirred at the reflux temperature for 4 hours, and then cooled to room temperature. Thereafter, to this, 2-naphthol (2.0 g) dissolved in ethanol (5 ml) was dropwise added in one hour. After stirring at room temperature for two hours, this mixture was heated to the reflux temperature, followed by stirring for additional 2 hours. The reaction mixture was filtrated and the filtrate was condensed to precipitate crystals. The crystals were filtrated for collection and recrystallized with dioxane-water to give intended crystals (0.59 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06551682B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-bcc37bbd64684155ad97be7a188f1593 |
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| Source note | uspto-grants-2003_04 |
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