Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | P-Toluic Acid | HCID 7470 | — |
| Reactant | 1,3,5-Trihydroxy-1,3,5-triazinane-2,4,6-trione | HCID 10419723 | — |
| Catalyst | Cobalt diacetate | HCID 6277 | — |
| Catalyst | Manganous Acetate | HCID 12525 | — |
| Catalyst | Titanium | HCID 23963 | — |
| Solvent | Water | HCID 962 | — |
| Product | P-Toluic Acid | HCID 7470 | — |
| Product | Terephthalic Acid | HCID 7489 | — |
Reaction Steps
In a 500-ml titanium autoclave equipped with a stirrer and a pressure gauge, 15.36 g of p-toluic acid, 104.0 g of acetic acid, 0.066 g of hexahydro-1,3,5-trihydroxy-1,3,5-triazine-2,4,6-trione (1,3,5-trihydroxyisocyanuric acid) (0.33% by mole relative to p-toluic acid), 0.112 g of cobalt(II) acetate.4H2O and 0.277 g of manganese(II) acetate.4H2O were placed. The autoclave was charged with 2 MPa of oxygen gas and 2 MPa of nitrogen gas and placed in a heated oil bath. The mixture was stirred at 150° C. for 1 hour. After the completion of the reaction, the autoclave was placed on cold water to cool down the reaction mixture quickly. The resulting mixture was analyzed by high performance liquid chromatography and was found to yield terephthalic acid in 63% yield at 68% conversion of p-toluic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091342B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-bd8297b3cf7f4124a97a04ca91aa86e8 |
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| Source note | uspto-grants-2006_08 |
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