Acrylamide → Acrylic acid n-decylacrylate acrylamide

HRID 1058495

Reaktionsgleichung

Reaktionsgleichung von HRID 1058495
[C:1]([OH:5])(=[O:4])[CH:2]=[CH2:3].[CH2:6]([O:16][C:17](=[O:20])[CH:18]=[CH2:19])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15].[C:21]([NH2:25])(=[O:24])[CH:22]=[CH2:23]>O1CCOCC1>[C:1]([OH:5])(=[O:4])[CH:2]=[CH2:3].[CH2:6]([O:16][C:17](=[O:20])[CH:18]=[CH2:19])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15].[C:21]([NH2:25])(=[O:24])[CH:22]=[CH2:23]

Komponenten

5

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

A solution was prepared of acrylic acid (10.0 g, 133 mmol), n-decylacrylate (3.0 g, 14.2 mmol) and acrylamide (3.0 g, 42.2 mmol) in dioxane (200 mL). After the solution was degassed with a rapid stream of nitrogen, AIBN (1.3 g) was added. The solution was degassed for a further thirty minutes and the reaction was then heated to 70° C. for 17 h. The polymer precipitated as a fibrous white solid as the reaction proceeded. The solution was cooled and the dioxane decanted. The residue was washed with ethyl acetate (600 mL) and the ethyl acetate was discarded. The polymer was finally washed with hexanes (300 mL) and dried in vacuo.

Aufarbeitung

  1. customAfter the solution was degassed with a rapid stream of nitrogen, AIBN (1.3 g)
  2. additionwas added
  3. customThe solution was degassed for a further thirty minutes
  4. customThe polymer precipitated as a fibrous white solid as the reaction
  5. temperatureThe solution was cooled
  6. customthe dioxane decanted
  7. washThe residue was washed with ethyl acetate (600 mL)
  8. washThe polymer was finally washed with hexanes (300 mL)
  9. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-c7d61ca8b2c14dea9cd0edf3b8d7d5fb
Quelldatensatz
uspto-grants-2003_02
Patentnummer
US06517826B1

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