Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrogen Sulfide | HCID 402 | — |
| Edukt | 6-Methoxy-alpha-tetralone | HCID 14112 | — |
| Edukt | Sulfur | HCID 5362487 | — |
| Produkt | 1-Naphthol | HCID 7005 | 34% |
Reaktionsschritte
A mixture of 50.0 g (0.28 mole) of 6-methoxy-1-tetralone and 9.2 g (0.29 mole) of elemental sulfur was stirred and heated at 250°-260° for three hours (until the evolution of hydrogen sulfide gas had ceased). The mixture was cooled and then subjected to bulb-to-bulb distillation. The distillate was dissolved in 300 ml of dichloromethane, and the solution was extracted with 1.0N potassium hydroxide solution (3×150 ml). The base extracts were combined, cooled in ice, and acidified with 10% hydrochloric acid to precipitate the crude naphthol product as a gum. Trituration of the gum with tert-butyl methyl ether yielded 16.8 g (34% yield) of the analytically pure naphthol, mp 84°-86° (a mp of 83°-84° is given by M. P. Sibi, J. W. Dankwardt, and V. Snieckus, J. Org. Chem., 51, 271 (1986)).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04767776 |
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| Quelldatensatz | uspto-grants-1988_08 |
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| ORD ID | ord-ec94404155954f4b8045d0970bcd1724 |
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| Quellennotiz | uspto-grants-1988_08 |
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