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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9756생성일: 2026년 10월 23일

Acetic Acid → Terephthalic Acid

https://huagongshe.com/ko/reaction/9756

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물WaterHCID 962—
반응물P-XyleneHCID 7809—
반응물1,3,5-Trihydroxy-1,3,5-triazinane-2,4,6-trioneHCID 10419723—
촉매Cobalt diacetateHCID 6277—
촉매Manganous AcetateHCID 12525—
생성물Terephthalic AcidHCID 748999%

반응 조건

온도150 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091342B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-6126e02d02c2469fb6ad8fa1a7eee34a
출처 메모uspto-grants-2006_08