HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251296Generated: October 26, 2026
4-Aminophenacylpyridinium chloride hydrochloride → 4-Aminophenacylpyridinium chloride
https://huagongshe.com/reaction/1251296
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Aminophenacylpyridinium chloride hydrochloride | HCID 22715291 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Aminophenacylpyridinium chloride | HCID 22715288 | — |
Reaction Steps
In 15 g of water, were dissolved 2 g of the thus-obtained 4-aminophenacylpyridinium chloride hydrochloride, and 4.5 g of a basic ion-exchange resin (Amberlite IRA400-OH) were added to the solution. After stirring the mixture, it was filtered to remove the ion-exchange resin, thereby obtaining an aqueous solution of 4-aminophenacylpyridinium chloride. The aqueous solution containing 1.3 g of 4-aminophenacylpyridinium chloride in 25 g of water was refluxed with 1 g of silver nitrate for 90 minutes. Precipitate formed was removed by filtration. To the resultant filtrate, were added 5 g of carbon black having a surface area of 200 m2/g and a DBPA of 122 ml/100 g, and the resultant mixture was heated to about 80° C. After 0.52 g of concentrated hydrochloric acid were added, a solution of sodium nitrite in a small amount of water was added, and the resultant dispersion was stirred for 1.5 hours. As a result, a diazonium salt with an NN+C6H4COCH2(N+C5H5) group having the following structure was formed and reacted to carbon black, thereby obtaining a product with a C6H4COCH2(N+C5H5) group bonded to the surface of the carbon black.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06342095B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-123919c8ed9844ca98f0178b598805bf |
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| Source note | uspto-grants-2002_01 |
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