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 | 0.6% |
| Product | Cyclohexanone | HCID 7967 | 5.2% |
Reaction Steps
To 20 ml of benzonitrile were added 10 mmol of cyclohexane, 1 mmol of N-hydroxyphthalimide and 0.05 mmol of cobalt acetate Co(OAc)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 5.2%), cyclohexanol (yield 0.6%) with a conversion of 6.3%. Adipic acid was not detected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05981420 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-0b1278dc64a14b1e8f3373bdd5dab5a6 |
| Source note | uspto-grants-1999_11 |