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 | 37% |
| Product | Cyclooctanol | HCID 12766 | 2.5% |
| Product | 1,4-Cyclooctanedione | HCID 521684 | 10% |
Reaction Steps
To 7.5 ml of acetic acid were added 336 mg (3.0 mmol) of cyclooctane, 60 mg (0.3 mmol) of N-hydroxysaccharin and 3.9 mg (0.015 mmol) of acetylacetonatocobalt Co(acac)2. The resultant mixture was stirred under an oxygen atmosphere at a temperature of 100° C. for 6 hours. The products in the reaction mixture were analysed by gas chromatography, with cyclooctane being transformed, with a conversion of 88%, into cyclooctanone (selectivity 42%, yield 37%), cyclooctanol (selectivity 3%, yield 2.5%), 1,4-cyclooctanedione (selectivity 11.5%, yield 10%) and octanediacid (selectivity 18%, yield 16%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07019175B2 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-addb1f619662412bbdf8ef7937111e84 |
| Source note | uspto-grants-2006_03 |