HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Cyclononanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Cyclononane | HCID 136143 | — |
| Product | Azelaic Acid | HCID 2266 | 42% |
| Product | Cyclononanone | HCID 76877 | 46% |
Reaction Steps
To 25 milliliters of acetic acid were added 1.26 grams (10 millimoles) of cyclononane, 0.13 gram (0.8 millimole) of N-hydroxyphthalimide and 0.015 gram (0.06 millimole) of Co(AA)2, and the resultant mixture was stirred in an oxygen atmosphere at a temperature of 100° C. for six hours. Products in the reaction mixture were analyzed by means of gas chromatography, which showed that cyclononane was transformed into cyclononanone (yield 46%) and azelaic acid (yield 42%) with a transformation rate of 92%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05958821 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-e48ee11f00ac4e63a57d171556889521 |
| Source note | uspto-grants-1999_09 |