Cyclohexane → Adipic Acid

HRID 890843

Reaction equation

HRID 890843 reaction equation
[CH2:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C([O:19][C:20]([C:22]1[CH:23]=[C:24]2[C:29](=[O:30])N(O)[C:26](=[O:27])[C:25]2=[CH:32][CH:33]=1)=[O:21])CCCCCCCCCCC.[N+]([O-])=[O:35]>C([O-])(=O)C.[Mn+2].C([O-])(=O)C>[CH:1]1([OH:19])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[C:22]1(=[O:35])[CH2:23][CH2:24][CH2:25][CH2:32][CH2:33]1.[C:20]([OH:19])(=[O:21])[CH2:22][CH2:23][CH2:24][CH2:25][C:26]([OH:27])=[O:35].[C:20]([OH:19])(=[O:21])[CH2:22][CH2:23][CH2:24][C:29]([OH:30])=[O:35]

Participants

8

Conditions

Temperature
80 °C

Procedure

A mixture of 4 ml (37 mmol) of cyclohexane, 0.1 mmol of 4-dodecyloxycarbonyl-N-hydroxyphthalimide, 0.01 mmol of acetylacetonatocobalt(II), 0.001 mmol of manganese(II) acetate and 0.06 mmol of nitrogen dioxide was stirred at 80° C. in an atmosphere of air (10 atm=1 MPa) for 2 hours and thereby yielded 0.30 mmol of cyclohexyl alcohol, 0.65 mmol of cyclohexanone, 0.10 mmol of adipic acid and 0.09 mmol of glutaric acid. The total amount of the four products was 1.14 mmol, and the amount of K/A oil was 0.95 mmol.

Sources & evidence

ORD record
ord-088c231e604341168519ced288e0b34e
Source dataset
uspto-grants-2006_02
Patent number
US06998491B2

Linked notes

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