HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942226Generated: October 25, 2026
Nitric Acid → 3-Acetylamino-adamantane-1-carboxylic acid
https://huagongshe.com/reaction/1942226
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1-Adamantanecarboxylic acid | HCID 13235 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Acetylamino-adamantane-1-carboxylic acid | HCID 2769714 | 73% |
Reaction Steps
To a 10-L reactor was added 1-adamantanecarboxylic acid (503 g, 2.79 mol; TCI America, Wellesley Hills, Mass., USA) and 70% nitric acid (400 mL, 6.72 mol), and the resulting suspension was cooled at 0° C. with a recirculating chiller. To the mixture was slowly added 98% sulfuric acid (3.00 L, 55.5 mol) at such a rate that the temperature was kept below 10° C. Once the addition completed, acetonitrile (2.00 L, 38.5 mol) was added at such a rate that the temperature was kept below 10° C. After all the acetonitrile was added, the reaction was stirred at 0° C. for 1 hour. The crude reaction was then added to a 20-L reactor filled with about 10-L of ice mixed with a small amount of water and the resulting mixture was stirred and allowed to warm to room temperature. The solids were then filtered and washed with water. More solids precipitated from the acidic aqueous layer and these were filtered as well and washed with water. The combined solid material was then dried under high vacuum at 50° C. for 2 days to afford 432 g (73%) of the title compound, 3-acetylamino-adamantane-1-carboxylic acid, as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389519B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-5485713c12764b90b6801a4e9d0f774c |
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| Source note | uspto-grants-2013_03 |
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