T. Iwahama et al., DIRECT CONVERSION OF CYCLOHEXANE INTO ADIPIC ACID WITH MOLECULAR-OXYGEN CATALYZED BY N-HYDROXYPHTHALIMIDE COMBINED WITH MN(ACAC)(2) AND CO(OAC)(2), Organic process research & development, 2(4), 1998, pp. 255-260
Direct conversion of cyclohexane into adipic acid was achieved by the
use of the radical catalyst, N-hydroxyphthalimide (NHPI), in the prese
nce of a small amount of a transition metal. For instance, cyclohexane
could be converted into adipic acid in 73% selectivity at 73% convers
ion under atmospheric oxygen (1 atm) in the presence of NHPI (10 mol %
) and Mn(acac)(2) (1 mol %) at 100 degrees C for 20 h, ESR measurement
s show that the formation of phthalimide N-oxyl generated from NHPI wi
th O-2 was assisted by Co(II) species. Thus, the oxidation of cyclohex
ane to adipic acid was found to be enhanced by the addition of a small
amount of Co(OAc)(2) to the NHPI/Mn(acac)(2) system. The NHPI-catalyz
ed oxidation of cyclohexane provides an attractive direct method which
has long been desired in the chemical industry for the manufacturing
of adipic acid. The present oxidation seems to be the first practical
environmentally friendly process, in which nitric acid is not used as
the oxidant, for the Production of adipic acid from cyclohexane.