Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Cyclooctene | HCID 638079 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 1,2-Epoxycyclooctane | HCID 67513 | 65% |
Reaction Steps
Hydrogen peroxide (30%, 2 ml) was added to a mixture of the catalyst from Example 48 (0.04 g) and cis-cyclooctene (1.4 g, 11.5 mmol) in tert-butanol (10 ml) at 30° C. under an atmosphere of nitrogen. The reaction mixture was stirred at 30° C. for 48 h under nitrogen. The catalyst was filtered off and washed well with ether (80 ml). The combined organic layers were washed well with water (2×40 ml) and then dried over magnesium sulphate. After filtration the solvent was removed under reduced pressure −20° C. at 50 mm of Hg—to afford 9-oxabicyclo[6.1.0] nonane as a white solid (0.95 g, 65%). M.p. 51° C., lit. m.p. 53–56° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07064226B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-6daaf30b19e849248cefd364b06165d4 |
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| Source note | uspto-grants-2006_06 |
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