HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Cyclooctanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Cyclooctanol | HCID 12766 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | Cyclooctanone | HCID 10403 | 71.1% |
Reaction Steps
10.6 g of stabilized IBX prepared as in Example 10 are suspended in 60 ml of N-methylpyrrolidone at 20° C., and 2 g of cyclooctanol are added dropwise while maintaining the temperature at from 20° C. to 25° C. After 2 hours, agitation, the medium is poured into a mixture of 130 ml of water and 80 ml of toluene; the pH of the aqueous phase is brought to approximately 7 by the addition of aqueous NaOH and the organic phase, after separation of the insoluble material formed and of the aqueous phase, is concentrated to give 1.4 g of pure cyclooctanone (NMR and GPC)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06462227B2 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-4ea1944d37164d8fb9561bcfa9f7b1be |
| Source note | uspto-grants-2002_10 |