Réaction #1328430

ord-13b1bdccc5684243bdc2c071e8df751a

Équation de réaction

Cc1ccc(C(=O)O)cc1
p-toluic acid
Cc1ccc(C(=O)O)cc1
p-toluic acid
O=O
oxygen
O=C(O)c1ccc(C(=O)O)cc1
terephthalic acid
CC(=O)ON1C(=O)c2ccccc2C1=O
N-acetoxyphthalimide
O=Cc1ccc(C(=O)O)cc1
4-carboxybenzaldehyde
Rendement 95.6%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

In a 500-ml titanium autoclave, 15.36 g (0.113 mol) of p-toluic acid, 1.16 g (5.65 mmol) of N-acetoxyphthalimide, 0.112 g (0.45 mmol) of cobalt(II) acetate tetrahydrate, 0.277 g (1.13 mmol) of manganese(II) acetate tetrahydrate and 107 g of acetic acid were placed, the resulting mixture was stirred at 150° C. in an atmosphere of a mixture of oxygen and nitrogen gases (1:1) [4 MPa (gauge pressure)] for 1 hour and thereby yielded terephthalic acid in a yield of 95.6% with a conversion from p-toluic acid of 97.4%. A small amount of 4-carboxybenzaldehyde was by-produced.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07115541B2uspto-grants-2006_10