Acrylamide → n-Decylacrylamide Acrylamid

HRID 1018395Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1018395
[Cl-].C[N+](C)(C)CCOC(=O)C=C.[CH2:13]([C:23](=[CH2:27])[C:24]([NH2:26])=[O:25])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22].[C:28]([NH2:32])(=[O:31])[CH:29]=[CH2:30]>C(O)(C)C>[CH2:13]([C:23](=[CH2:27])[C:24]([NH2:26])=[O:25])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22].[C:28]([NH2:32])(=[O:31])[CH:29]=[CH2:30]

Komponenten

5

Edukt 3

HCID 6579AcrylamideHCID 162071Ethanaminium, N,N,N-trimethyl-2-[(1-oxo-2-propen-1-yl)oxy]-, chloride (1:1)HCID 212758792-Methylidenedodecanamide

Produkt 1

HCID 21275878n-Decylacrylamide Acrylamid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3776IsopropanolLösungsmittel

Reaktionsbedingungen

Temperatur
75 °C

Versuchsvorschrift

To a 500 mL round-bottom, three-neck flask fitted with a thermocouple, reflux condenser, and septum was added 150 mL of isopropanol followed by 16.13 g of a 50% aqueous solution of 2-trimethylammonioethylacrylate chloride, 8.06 g of n-decylacrylamide, and 8.06 g of acrylamide. The solution was purged with nitrogen for 1 hour and 0.5 g AIBN was added. The mixture was purged for ˜15 minutes until all of the AIBN dissolved. The solution was heated to 75° C. under nitrogen for 16 hours.

Aufarbeitung

  1. customTo a 500 mL round-bottom, three-neck flask fitted with a thermocouple
  2. temperaturereflux condenser
  3. customThe solution was purged with nitrogen for 1 hour
  4. addition0.5 g AIBN was added
  5. customThe mixture was purged for ˜15 minutes until all of the AIBN
  6. dissolutiondissolved

Quellen und Nachweise

ORD-Eintrag
ord-8eb5784645d9498ca1bdc64fae527ecf
Quelldatensatz
uspto-grants-2002_11
Patentnummer
US06482402B1

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