HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxygen → 2-Cyclohexen-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Cyclohexene | HCID 8079 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Cyclohexen-1-OL | HCID 13198 | 1% |
| Product | 2-Cyclohexen-1-one | HCID 13594 | 4% |
Reaction Steps
To 25 milliliters of acetonitrile, were added 1.64 grams (20 millimoles) of cyclohexene, and azobisisobutyronitrile (5 mole percent). The resultant mixture was stirred in an oxygen atmosphere at a temperature of 90° C. for 4 hours. In analysis of the product in the reaction mixture with gas chromatography, cyclohexene was transformed into 2-cyclohexen-1-one (cyclohexene-based selectivity 12%, yield 4%) and 2-cyclohexen-1-ol (cyclohexene-based selectivity 3%, yield 1%) with a transformation rate of 34 percent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05958821 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-649c20d7c97a4a1681038222a93455ec |
| Source note | uspto-grants-1999_09 |