Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Naphthol | HCID 7005 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2-Bromo-1-naphthol | HCID 150849 | — |
| Edukt | N-bromo-t-butylamine | HCID 11789384 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | 2-Bromo-1-methoxynaphthalene | HCID 12612830 | — |
Reaktionsschritte
1-naphthol was converted into 2-bromo-1-naphthol by reaction with a slurry of N-bromo-t-butylamine at -78° C. according to the procedure described in Pearson, Wysong, Breder, J. Org. Chem. 32, 2358 (1967). To a solution of 1 mole (crude) of the bromonaphthol in 750 mL of acetone was added 175 g of potassium carbonate. Over a 2-hous period, 95 mL of dimethylsulate was added dropwise to the mechanically stirred reaction mixture. The resulting slurry was stirred at 25° C. overnight. The solids were filtered and the solution was stripped to yield a dark brown oil. Initial purification was accomplished by vacuum distillation (80°-120° C., 0.2 Torr) followed by further purification by HPLC with hexane to yield 145 g of 2-bromo-1-methoxynaphthalene as a pale yellow oil. NMR confirmed the structure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05244771 |
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| Quelldatensatz | uspto-grants-1993_09 |
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| ORD ID | ord-352027f5ace04caca5d1f5c9a25194cf |
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| Quellennotiz | uspto-grants-1993_09 |
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