Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrogen Peroxide | HCID 784 | — |
| Edukt | 1-Cyclooctene | HCID 13609 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 1,2-Epoxycyclooctane | HCID 67513 | 89,3% |
Reaktionsschritte
Crosslinked polystyrene-divinylbenzene beads substituted in the phenyl rings by arsono groups (Polymer II of Example 2 (B) above, containing 0.25 mmole As) was added to a two phase system of 1.7 g of 30% aqueous H2O2 (15 mmoles of H2O2) and cyclooctene (7.5 mmoles) in chloroform (7 ml). The mixture was heated in a closed thick-walled tube at 70° C. for 45 hours. Cyclooctene oxide (6.7 mmol, 89% yield) was obtained after 45 hours. The polymer was then filtered and reused with no apparent loss of activity (90% yield after 55 hours at 70° C.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04286068 |
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| Quelldatensatz | uspto-grants-1981_08 |
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| ORD ID | ord-4a684355f1b447ddb4c15057a804cb69 |
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| Quellennotiz | uspto-grants-1981_08 |
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