Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Cupric acetate | HCID 8895 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86758610 | HCID 86758610 | — |
Reaction Steps
After cyclohexane (40 mmol), Cu(OAc)2 (2.5×10−3 mmol), acetaldehyde (4.0 mmol), benzonitrile (2.5 ml) and dichloromethane (2.5 ml) were charged into a 25-ml eggplant-type flask, and an oxygen balloon was attached to the flask for supplying oxygen at 1 atm. Then, the mixture was stirred at 25° C. for 48 hours. The reaction mixture was analyzed with the gas chromatography, which revealed that the yield of cyclohexanol was 9% (relative to 1 equivalent of acetaldehyde), that of cyclohexanone was 29% (relative to 2 equivalents of acetaldehyde), and the turnover number of the catalyst was 375.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06482989B2 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-850cc459c95344ea9d898676cc7a9aaf |
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| Source note | uspto-grants-2002_11 |
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