HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzonitrile → Cyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | Cyclohexanol | HCID 7966 | 1% |
| Product | Cyclohexanone | HCID 7967 | 10% |
Reaction Steps
To 20 ml of benzonitrile were added 10 mmol of cyclohexane, 1 mmol of N-hydroxyphthalimide, 0.01 mmol of cobalt acetate Co(OAc)2, and 0.05 mmol of acetylacetonatocobalt Co(AA)2 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%) and cyclohexanol (yield 1%) with a conversion of 12%. Adipic acid was not detected. The selectivity of K/A oil was 93% based on the consumed cyclohexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05981420 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-65977e8ac92d4e15b1f64bae111a8cc9 |
| Source note | uspto-grants-1999_11 |