Reaktion #324369

ord-934bc97a98874649a165d5e8a6cf5c39

Reaktionsgleichung

C=C(C)C(=O)NCCCN(C)C
N-[3-(dimethylamino)propyl]methacrylamide
O=S1(=O)CCCCO1
butanesultone
CC(C)=O
acetone
CO
methanol
C=C(C)C(=O)NCCC[N+](C)(C)CCCCS(=O)(=O)[O-]
4-sulfonatobutyl[3-(methacryloylamino)propyl]dimethylammonium
Ausbeute 85.5%

Lösungsmittel

Reaktionsbedingungen

Temperatur
70°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto cooling, to the reaction mixture
  2. 2
    FiltrationThe crystals deposited were collected by filtration
  3. 3
    Waschenthoroughly washed with acetone

Vorschrift

In 380 ml of acetonitrile were dissolved 130 g (0.764 mol) of N-[3-(dimethylamino)propyl]methacrylamide, 104 g of butanesultone and 234 mg of 4-hydroxy-2,2,6,6-tetramethylpiperidinoxy and the solution was heated at 70° C. for 6 hours. After allowing to cooling, to the reaction mixture were added 1,350 ml of acetone and 150 ml of methanol and the mixture was stirred at room temperature for one hour. The crystals deposited were collected by filtration and thoroughly washed with acetone to obtain 200.0 g (yield: 85%) of 4-sulfonatobutyl[3-(methacryloylamino)propyl]dimethylammonium.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08642243B2uspto-grants-2014_02