참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Oxygen | HCID 977 | — |
| 반응물 | P-Toluic Acid | HCID 7470 | — |
| 반응물 | 1,3,5-Triacetoxy-hexahydro-1,3,5-triazine-2,4,6-trione | HCID 11301124 | — |
| 촉매 | Cobalt diacetate | HCID 6277 | — |
| 촉매 | Manganous Acetate | HCID 12525 | — |
| 촉매 | Titanium | HCID 23963 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | P-Toluic Acid | HCID 7470 | — |
| 생성물 | Terephthalic Acid | HCID 7489 | — |
반응 단계
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, 0.114 g of 1,3,5-triacetoxy-hexahydro-1,3,5-triazine-2,4,6-trione (1,3,5-triacetoxyisocyanuric 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 90% yield at 93% conversion of p-toluic acid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07091342B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-3d5750931bd44381b0102746045a956c |
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| 출처 메모 | uspto-grants-2006_08 |
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