HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Adamantanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Adamantane | HCID 9238 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Product | Adamantanone | HCID 64151 | 30% |
| Product | 1-Hydroxyadamantan-2-one | HCID 10964884 | 15% |
Reaction Steps
To 25 ml of acetic acid were added 10 mmol of adamantane, 1 mmol of N-hydroxyphthalimide and 0.3 mmol of phosphovanadomoribdic acid (PV5Mo7O40.30H2), and the resultant mixture (pH 1.2) was stirred under an oxygen atmosphere at a temperature of 75° C. for 6 hours. The products in the reaction mixture were analyzed by gas chromatography, and, as a result, adamantane was converted into adamantanone (yield 30%) and 1-hydroxyadamantanone (yield 15%) with a conversion of 77%. Incidentally, excepting the above, 1-adamantanol (yield 16%), 1,3-adamantanediol (yield 8%) and other products (polyketone such as adamantanedione) (yield 8%) were formed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06232258B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-4a9f43127db9410bb9d3999bfd3b273f |
| Source note | uspto-grants-2001_05 |