Reaktion #9852

Reaktionsgleichung

hexahydro-1,3,5-trihydroxy-1,3,5-triazine-2,4,6-trione

p-xylene

water

p-xylene

acetic acid

→

terephthalic acid

Ausbeute 99.0%

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONThe autoclave was charged with 2 MPa of air
2. 2
   Sonstigeplaced in a heated oil bath
3. 3
   SonstigeAfter the completion of reaction
4. 4
   Temperaturto cool down the reaction mixture quickly

Vorschrift

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.

Quelle