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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182343Generated: November 4, 2026

Acetic Acid → Terephthalic Acid

https://huagongshe.com/reaction/1182343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantP-XyleneHCID 7809—
Reactant1,3,5-Trihydroxy-1,3,5-triazinane-2,4,6-trioneHCID 10419723—
CatalystCobalt diacetateHCID 6277—
CatalystManganous AcetateHCID 12525—
ProductTerephthalic AcidHCID 748999%

Reaction Conditions

Temperature150 °C

Reaction Steps

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.4 H2O, 0.003 g of manganese(II) acetate.4 H2O 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288649B2
Source datasetuspto-grants-2007_10
ORD IDord-849413584eb34ae78a901248557f7093
Source noteuspto-grants-2007_10