HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Acetic Acid → Terephthalic Acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Oxygen | HCID 977 | — |
| Edukt | P-Xylene | HCID 7809 | — |
| 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 | — |
| Produkt | Terephthalic Acid | HCID 7489 | 97% |
Reaktionsschritte
A mixture of 0.212 g of p-xylene, 0.011 g of hexahydro-1,3,5-trihydroxy-1,3,5-triazine-2,4,6-trione (3% by mole relative to p-xylene), 0.013 g of N,N′-diacetoxypyromellitdiimide (2% by mole relative to p-xylene), 5 g of acetic acid, 0.003 g of cobalt(II) acetate.4H2O and 0.003 g of manganese(II) acetate.4H2O was stirred at 100° C. in an atmosphere of oxygene gas (1 atm=0.1 MPa) for 14 hours. The resulting product in the reaction mixture was analyzed by high performance liquid chromatography and was found to yield terephthalic acid in 97% yield at 100% conversion of p-xylene.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07091342B2 |
| Quelldatensatz | uspto-grants-2006_08 |
| ORD ID | ord-29285ec6745d475093824ce4bb81f136 |
| Quellennotiz | uspto-grants-2006_08 |