HuagongsheHuagongshe Chemistry Print Report · For research reference only
Adipic Acid → Cyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Adipic Acid | HCID 196 | — |
| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | Cyclohexanol | HCID 7966 | 0.8% |
| Product | Cyclohexanone | HCID 7967 | 10% |
Reaction Steps
To 10 ml of benzonitrile were added 10 mmol of cyclohexane, 1 mmol of N-hydroxyphthalimide, 0.01 mmol of cobalt acetate Co(OAc)2, and 0.1 mmol of acetylacetonatochromium Cr(AA)3 and the resultant mixture was stirred under an oxygen atmosphere at a temperature of 75° C. for 16 hours. The products in the reaction mixture were analyzed by gas chromatography, and, as a result, cyclohexane was converted into cyclohexanone (yield 10%), cyclohexanol (yield 0.8%) and adipic acid (trace amount) with a conversion of 33%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05981420 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-7b1c7b258c74409690236d81c2fa4fb0 |
| Source note | uspto-grants-1999_11 |