Hydrochloric Acid → N-Hexadecylacrylamide

HRID 841105

Reaktionsgleichung

Reaktionsgleichung von HRID 841105
[CH2:1](Cl)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].[C:18]([NH2:22])(=[O:21])[CH:19]=[CH2:20].[Cl-].[Al+3].[Cl-].[Cl-].Cl>O.CC(C)=O>[CH2:1]([NH:22][C:18](=[O:21])[CH:19]=[CH2:20])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]

Komponenten

7

Versuchsvorschrift

In a 250 ml capacity conical flask 13 g cetyl chloride (0.05 M), 3.5 g acrylamide (0.05 M) and 50 ml acetone were placed to obtain a clear solution. The solution was stirred with a magnetic needle at room temperature. 6.5 g anhydrous aluminium chloride (0.05 M) was added and the reaction mixture was stirred at room temperature. After 5 to 10 minutes of stirring, vigorous evolution of hydrogen chloride took place which ceased after about 5 minutes. Temperature of the reaction mixture was raised to 40 to 50° C. It was then cooled to room temperature and poured into 500 ml cold water. White product was precipitated. The product was isolated and purified by reprecipitation from acetone into cold water.

Aufarbeitung

  1. customto obtain a clear solution
  2. stirringthe reaction mixture was stirred at room temperature
  3. stirringAfter 5 to 10 minutes of stirring
  4. temperatureTemperature of the reaction mixture was raised to 40 to 50° C
  5. temperatureIt was then cooled to room temperature
  6. customWhite product was precipitated
  7. customThe product was isolated
  8. custompurified by reprecipitation from acetone into cold water

Quellen und Nachweise

ORD-Eintrag
ord-eaf1af5461a34344a0ac78c0f3a7fbe9
Quelldatensatz
uspto-grants-2002_04
Patentnummer
US06369249B1

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