Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | 2-Nitrotoluene | HCID 6944 | — |
| Edukt | 1,3,5-Trihydroxy-1,3,5-triazinane-2,4,6-trione | HCID 10419723 | — |
| Katalysator | Cobalt diacetate | HCID 6277 | — |
| Katalysator | Manganous Acetate | HCID 12525 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-Nitrotoluene | HCID 6944 | — |
| Produkt | 2-Nitrobenzoic acid | HCID 11087 | — |
Reaktionsschritte
In an autoclave, 0.274 g of 2-nitrotoluene, 0.018 g of hexahydro-1,3,5-trihydroxy-1,3,5-triazine-2,4,6-trione (5% by mole relative to 2-nitrotoluene), 5 g of acetic acid, 0.003 g of cobalt (II) acetate.4H2O, 0.001 g of manganese(II) acetate.4H2O and 0.018 g of NO2 were placed. The autoclave was charged with 1 MPa of air and placed in a heated oil bath. The mixture was stirred at 150° C. for 14 hours. After the completion of reaction, the autoclave was placed on cold water to cool down the reaction mixture quickly. The resulting mixture was analyzed by gas chromatography and was found to yield 2-nitrobenzoic acid in 62% yield at 67% conversion of 2-nitrotoluene.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07091342B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-98cca51794be4ca59ebc9de69d50807e |
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| Quellennotiz | uspto-grants-2006_08 |
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