Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1182328Erstellt: 27. Oktober 2026

Acetic Acid → P-Toluic Acid

https://huagongshe.com/reaction/1182328

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—
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-toluicacid, 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 4 H2O and 0.277 g of manganese(II) acetate 4 H2O 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
PatentnummerUS07288649B2
Quelldatensatzuspto-grants-2007_10
ORD IDord-abca0c6b5bbc43b08c2a87a32187104c
Quellennotizuspto-grants-2007_10