HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → 3-Hydroxyadamantane-1-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 1-Adamantanecarboxylic acid | HCID 13235 | — |
| Reactant | 1-Adamantanol | HCID 64152 | — |
| Product | 3-Hydroxyadamantane-1-carboxylic acid | HCID 2736518 | 25.2% |
Reaction Steps
The same operations as conducted in Example 1 were repeated, except that the reaction mixture temperature after dropwise addition of nitric acid was set to 80° C. In the first carboxylation reaction step, the conversion of 1-adamantanol was found to be 99.0% and 1-adamantane carboxylic acid was generated in a reaction yield of 97%. In the second oxidation reaction step, the conversion of 1-adamantane carboxylic acid was found to be 98.0% and white crystals of 3-hydroxy adamantane-1-carboxylic acid (9.8 g, yield: 25.2%) were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09051256B1 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-3d7f983c596946d2a3f536f713f56c12 |
| Source note | uspto-grants-2015_06 |