Reaktion #1328431

ord-f2cea52cec5f45c8839e32de4bf6b7a9

Reaktionsgleichung

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
Ausbeute 74.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

In a 500-ml titanium autoclave, 15.36 g (0.113 mol) of p-toluic acid, 0.232 g (1.13 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 170° 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 74.4% with a conversion from p-toluic acid of 77.5%. A small amount of 4-carboxybenzaldehyde was by-produced.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07115541B2uspto-grants-2006_10