HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Cyclooctanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Cyclooctane | HCID 9266 | — |
| Reactant | HCID 10465358 | HCID 10465358 | — |
| Product | Cyclooctanone | HCID 10403 | 19% |
| Product | Cyclooctanol | HCID 12766 | 8% |
| Product | 1,4-Cyclooctanedione | HCID 521684 | 2% |
Reaction Steps
To 27.5 ml of acetic acid were added to 336 mg (3.0 mmol) of cyclooctane, 60 mg (0.3 mmol) of N-hydroxysaccharin and 3.7 mg (0.015 mmol) of Co(OAc)2.4H2O. The resultant mixture was stirred under an oxygen atmosphere at a temperature of 50° C. for 9 hours. The products in the reaction mixture were analysed by gas chromatography, with cyclooctane being transformed, with a conversion of 43.5%, into cyclooctanone (selectivity 43.5%, yield 19%), cyclooctanol (selectivity 18%, yield 8%), 1,4-cyclooctanedione (selectivity 4.5%, yield 2%) and octanediacid (selectivity 23%, yield 10%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07019175B2 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-cf40a610aabf4c88a399cd8f7f629e73 |
| Source note | uspto-grants-2006_03 |