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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminophenacylpyridinium chloride hydrochlorideHCID 22715291—
SolventWaterHCID 962—
Product4-Aminophenacylpyridinium chlorideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342095B1
Source datasetuspto-grants-2002_01
ORD IDord-123919c8ed9844ca98f0178b598805bf
Source noteuspto-grants-2002_01