Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrogen Bromide | HCID 260 | — |
| Edukt | 6-Amino-1,2,3,4-tetrahydronaphthalen-1-one | HCID 339537 | — |
| Edukt | Sodium Nitrite | HCID 23668193 | — |
| Katalysator | copper(I) bromide | HCID 24593 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 6-Bromo-1-tetralone | HCID 10105069 | — |
Reaktionsschritte
To a suspension of 6-amino-3,4-dihydro-2H-naphthalen-1-one (20.5 g, 127 mmol) in 25% HBr (aq) (1017 ml) at 0° C. was added a solution of sodium nitrite (10.53 g, 153 mmol) in water (50 ml) dropwise at a rate as to maintain the temperature below 3°. The cooled reaction mixture was then added to a cooled solution of copper(I) bromide (18.79 g, 131 mmol) in HBr (98 ml, 865 mmol). When the addition was done, the reaction mixture was stirred at 0° C. for 1 h, then warmed to rt. Water (380 mL) was added and the product was extracted with a mixture of Et2O/EtOAc (8:2, 3×). The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo to give a dark brown crude oil. The crude was purified by distillation (3 mm Hg) to give 16.415 g of 6-bromo-3,4-dihydro-2H-naphthalen-1-one.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08865701B2 |
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| Quelldatensatz | uspto-grants-2014_10 |
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| ORD ID | ord-8250d8215efc4d1f8c8ced1ec71915f9 |
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| Quellennotiz | uspto-grants-2014_10 |
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