HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1,3-Adamantanediol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Adamantane | HCID 9238 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Product | Adamantanone | HCID 64151 | 6% |
| Product | 1-Adamantanol | HCID 64152 | 39% |
| Product | 1,3-Adamantanediol | HCID 573829 | 49% |
Reaction Steps
To 25 ml of acetic acid were added 10 mmol of adamantane, 1 mmol of N-hydroxyphthalimide and a binary co-catalyst [0.1 mmol of acetylacetonatocobalt Co(AA)3 and 0.4 mmol of acetylacetonatoiron Fe(AA)3 ]and the resultant mixture 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 1-adamantanol (yield 39%) , 1,3-adamantanediol (yield 49%) and adamantanone (yield 6%) with a conversion of 99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05981420 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-5300959e4d8948eaa6388e6bd076c7a0 |
| Source note | uspto-grants-1999_11 |