HuagongsheHuagongshe Chemistry Print Report · For research reference only
Di-tert-butyl peroxide → Cyclooctane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Di-tert-butyl peroxide | HCID 8033 | — |
| Reactant | Cyclooctane | HCID 9266 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Product | Cyclooctane | HCID 9266 | — |
| Product | Cyclooctanone | HCID 10403 | — |
| Product | Cyclooctanol | HCID 12766 | — |
Reaction Steps
2 mmol of N-hydroxyphthalimide and 4 mmol of di-tert-butyl peroxide are added at a temperature of 130° C. to 200 mmol of cyclooctane in a round-bottomed flask having an attached reflux condenser. Air at approximately 15 l/h is passed through the reaction mixture for 8 hours at said temperature. Cyclooctanol is obtained at a selectivity of 15% and cyclooctanone at a selectivity of 43%, at a cyclooctane conversion rate of 51%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06852893B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-0e763f365a82438db6bb844e525df0ba |
| Source note | uspto-grants-2005_02 |