2-Acrylamido-2-methyl-1-propanesulfonic acid → Ammonium acryloyldimethyltaurate

HRID 1614837

Reaktionsgleichung

Reaktionsgleichung von HRID 1614837
COCCOCC[N:8](CCOCCOC)CCOCCOC.[C:23]([NH:27][C:28]([CH3:35])([CH3:34])[CH2:29][S:30]([OH:33])(=[O:32])=[O:31])(=[O:26])[CH:24]=[CH2:25]>>[NH4+:8].[C:23]([NH:27][C:28]([CH3:35])([CH3:34])[CH2:29][S:30]([O-:33])(=[O:31])=[O:32])(=[O:26])[CH:24]=[CH2:25]

Komponenten

3

Edukt 2

HCID 653602-Acrylamido-2-methyl-1-propanesulfonic acidHCID 112414Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-

Produkt 1

HCID 6850854Ammonium acryloyldimethyltaurateAusbeute 99 %

Versuchsvorschrift

A nitrogen purged 50 ml schlenk flask was charged with freshly distilled tris[2-(2-methoxyethoxy)-ethyl]amine (1.69 g, 5.24 mmol) and 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS) (1.09 g, 5.24 mmol) and stirred at ambient temperature for 8 hr or until completely dissolved. Total dissolution completes formation of the AMPS-ammonium salt monomer as a transparent light amber oil in a 99% yield which was used immediately without further purification.

Aufarbeitung

  1. customA nitrogen purged 50 ml schlenk flask
  2. dissolutionuntil completely dissolved
  3. dissolutionTotal dissolution
  4. customwas used immediately without further purification

Quellen und Nachweise

ORD-Eintrag
ord-d7f97ed05a4c4b279cb92f906eed8229
Quelldatensatz
uspto-grants-2014_07
Patentnummer
USRE044988E1

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