DIRECT CONVERSION OF CYCLOHEXANE INTO ADIPIC ACID WITH MOLECULAR-OXYGEN CATALYZED BY N-HYDROXYPHTHALIMIDE COMBINED WITH MN(ACAC)(2) AND CO(OAC)(2)

Citation
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
Citations number
43
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Medicinal
ISSN journal
10836160
Volume
2
Issue
4
Year of publication
1998
Pages
255 - 260
Database
ISI
SICI code
1083-6160(1998)2:4<255:DCOCIA>2.0.ZU;2-C
Abstract
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.