Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Cyclohexene | HCID 8079 | — |
| Product | HCID 18172638 | HCID 18172638 | 53% |
Reaction Steps
Cyclohexene (0.05 mole; 4.1 g) and MoO2(acac)2 (0.5 mmol; 162 mg) were dissolved in anhydrous 1-butanol (30 ml). There was then added one spatulaful of dry mole sieve (4 Å) followed by heating to 60° C. There was added 0.08 ml of BF3 etherate (≈0.5 mmol) followed by the dropwise addition of anhydrous tert-butyl hydroperoxide (0.06 mole; 3M in decane, 20 ml) in 30 minutes. The mixture was allowed to afterreact for 16 hours. The product then was further treated as described in Example 1. According to GC analysis, the 2-butoxy-cyclohexanol yield was 53% of theoretical, relative to cyclohexene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06608230B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-ed0f1bf10f1845229782b0ac77917398 |
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| Source note | uspto-grants-2003_08 |
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