Reaktion #1583846

ord-e9383888ac65474884d3b8d93eb95da7

Reaktionsgleichung

CCCCCCCCCCCC(=O)NCCCC[C@H](N)C(=O)OCC
Nε-Lauroyl-L-lysine ethyl ester
CCCCCCCCCCC1CC(=O)OC1=O
n-decyl succinic anhydride
CCCCCCCCCCCC(=O)NCCCC[C@H](NC(=O)CC(CCCCCCCCCC)C(=O)O)C(=O)OCC
Nε-lauroyl-Nα-(3-carboxytridecanoyl)-L-lysine ethyl ester
Ausbeute 85.9%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe obtained white turbid solution was heated
  2. 2
    Temperaturcooled in a freezer
  3. 3
    Sonstigeto give crystals
  4. 4
    FiltrationThe mixture was filtered
  5. 5
    Sonstigedried
  6. 6
    Sonstigerecrystallized

Vorschrift

Nε-Lauroyl-L-lysine ethyl ester (29.9 g) was dissolved in dehydrated dichloromethane (650 ml), n-decyl succinic anhydride (21.2 g) was added, and the mixture was stirred at room temperature for 24 hr. The obtained white turbid solution was heated and cooled in a freezer to give crystals. The mixture was filtered, dried, and recrystallized to give Nε-lauroyl-Nα-(3-carboxytridecanoyl)-L-lysine ethyl ester (43 g, yield 85%). 4 g thereof was dissolved in distilled ethanol (100 ml), and 4M aqueous NaOH solution (1.68 ml) was added with stirring. The mixture was stirred at room temperature for 3 hr, filtered, dried under reduced pressure, and recrystallized. yield 4.1 g, 97%.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09198846B2uspto-grants-2015_12