4-Aminophenacylpyridinium chloride hydrochloride → 4-Aminophenacylpyridinium chloride

HRID 1251296Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1251296
[ClH:1].[Cl-].[NH2:3][C:4]1[CH:18]=[CH:17][C:7]([C:8](=[O:16])[CH2:9][N+:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:6][CH:5]=1>O>[Cl-:1].[NH2:3][C:4]1[CH:5]=[CH:6][C:7]([C:8](=[O:16])[CH2:9][N+:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:17][CH:18]=1

Komponenten

3

Versuchsvorschrift

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.

Aufarbeitung

  1. additionwere added to the solution
  2. filtrationwas filtered
  3. customto remove the ion-exchange resin

Quellen und Nachweise

ORD-Eintrag
ord-123919c8ed9844ca98f0178b598805bf
Quelldatensatz
uspto-grants-2002_01
Patentnummer
US06342095B1

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