Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
ReactantAcetonitrileHCID 6342—
Reactant1-Adamantanecarboxylic acidHCID 13235—
SolventWaterHCID 962—
Product3-Acetylamino-adamantane-1-carboxylic acidHCID 276971473%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389519B2
Source datasetuspto-grants-2013_03
ORD IDord-5485713c12764b90b6801a4e9d0f774c
Source noteuspto-grants-2013_03