참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | P-Xylene | HCID 7809 | — |
| 반응물 | 1,3,5-Trihydroxy-1,3,5-triazinane-2,4,6-trione | HCID 10419723 | — |
| 촉매 | Cobalt diacetate | HCID 6277 | — |
| 촉매 | Manganous Acetate | HCID 12525 | — |
| 생성물 | Terephthalic Acid | HCID 7489 | 99% |
반응 단계
In an autoclave, 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), 5 g of acetic acid, 0.003 g of cobalt(II) acetate.4H2O, 0.003 g of manganese(II) acetate.4H2O and 0.001 g of zirconium oxyacetate were placed. The autoclave was charged with 2 MPa of air and placed in a heated oil bath. The mixture was stirred at 150° C. for 12 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 high performance liquid chromatography and was found to yield terephthalic acid in 99% yield at 100% conversion of p-xylene.
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-6126e02d02c2469fb6ad8fa1a7eee34a |
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| 출처 메모 | uspto-grants-2006_08 |
|---|