Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl orthoformate | HCID 31214 | — |
| Edukt | 2-Methoxy-6-nitrophenol | HCID 10942855 | — |
| Katalysator | p-Toluenesulfonic acid | HCID 6101 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 7-Methoxybenzo[d]oxazole | HCID 18465686 | 85,2% |
Reaktionsschritte
A mixture of 2-nitro-6-methoxyphenol (2.62 g, 15.5 mmol) (EP 333176) and 10% Palladium on carbon (130 mg) in ethanol (50.0 ml) was stirred under an atmosphere of H2 f or 75 min. The mixture was filtered through Celite® then immediately treated with p-toluenesulphonic acid (32.0 mg) and triethylorthoformate (6.45 ml, 38.8 mmol) then heated under reflux under an atmosphere of N2. After 20 h p-toluenesulphonic acid (30.0 mg) and triethylorthoformate (6.45 ml, 38.8 mmol) were added. After a total of 44 h heating, the reaction was allowed to cool and reduced in vacuo. The resulting residue was purified by flash chromatography (25:75 ethyl acetate/hexane) to give 1.97 g (85%) of the title compound as a yellow solid: m.p. 28-31° C.; IR (film) 1629, 1497, 1434, 1285, 1097;
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07288624B2 |
|---|
| Quelldatensatz | uspto-grants-2007_10 |
|---|
| ORD ID | ord-4ea65bbe55924f54bef5ae044aca419b |
|---|
| Quellennotiz | uspto-grants-2007_10 |
|---|