Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2'-Bipyridine | HCID 1474 | — |
| Reactant | 4-tert-Butylcyclohexanone | HCID 7392 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178445811 | HCID 178445811 | 8.6% |
| Product | HCID 178445812 | HCID 178445812 | 21.1% |
Reaction Steps
RuClCp* (cod) (3.8 mg, 0.01 mmol), KOH (0.04 mmol), 2,2′-bipyridyl (3.1 mg, 0.02 mmol) and 4-t-butylcyclohexanone (385.63 mg, 2.5 mmol) were dissolved into 10 ml of 2-propanol, and deaerated by argon substitution, after which the total amount of the resulting mixture was transferred into a 100-milliliter metallic autoclave. Then, the reaction was started at room temperature (28° C.) while conducting argon substitution. After the reaction solution was stirred for 18 hours, the reaction produces, cis-4-t-butylcyclohexanol (yield 8.6%) and trans-4-t-butylcyclohexanol (yield 21.1%), were identified and quantitatively determined by TLC monitor (silica gel: n-hexane/ethyl acetate=4/1) and gas chromatography of the reaction solution. Here, 35.0% of the raw material, 4-t-butylcyclohexanone, was recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06476278B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-99519967588c43488394062fde61dfd4 |
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| Source note | uspto-grants-2002_11 |
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