HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-Acetylamino-3-adamantanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | 1-Acetamidoadamantane | HCID 64153 | — |
| Catalyst | HCID 178528047 | HCID 178528047 | — |
| Product | 1-Acetylamino-3-adamantanol | HCID 2842792 | — |
| Product | N-(4-oxo-1-adamantyl)acetamide | HCID 5338964 | — |
| Product | 1-Acetylamino-3,5-adamantanediol | HCID 22463599 | — |
Reaction Steps
Mixture of 10 mmole 1-acetylaminoadamantane (Aldrich chemical Company, Inc.), 1 mmole of N-hydroxyphthalimide (NHPI), 0.05 mmole of vanadium (III) acetylacetonato (V(AA)3) and 25 mL of acetic acid was stirred under an oxygen atmosphere and the conditions represented in Table 1 (temperature and time). The products in the reaction mixture were analyzed by gas chromatography, and, as a result, 1-acetylamino-3-adamantanol (compound 1), 1-acetylamino-3,5-adamantanediol (compound 2) and 1-acetylamino-4-adamantanone (compound 3) were obtained with conversions and yields represented in Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE039744E1 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-dcd126749f3d4ea2b0d061a0a837bdbc |
| Source note | uspto-grants-2007_07 |