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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9741Erstellt: 23. Oktober 2026

Acetic Acid → P-Toluic Acid

https://huagongshe.com/de/reaction/9741

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktOxygenHCID 977—
EduktP-Toluic AcidHCID 7470—
Edukt1,3,5-Triacetoxy-hexahydro-1,3,5-triazine-2,4,6-trioneHCID 11301124—
KatalysatorCobalt diacetateHCID 6277—
KatalysatorManganous AcetateHCID 12525—
KatalysatorTitaniumHCID 23963—
LösungsmittelWaterHCID 962—
ProduktP-Toluic AcidHCID 7470—
ProduktTerephthalic AcidHCID 7489—

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091342B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-3d5750931bd44381b0102746045a956c
Quellennotizuspto-grants-2006_08