Reaktion #1583847

ord-7878d13113e443cd9f33911ff8643462

Reaktionsgleichung

CCCCCCCCCCCC(=O)NCCCC[C@H](N)C(=O)O
Nε-Lauroyl-L-lysine
CCOCC
ether
CCOCC
ether
Cl
hydrochloric acid
CCCCCCCCCCCC(=O)NCCCC[C@H](NC(=O)CCCCC(=O)O)C(=O)O
Nε-lauroyl-Nα-(5-carboxypentanoyl)-L-lysine
Ausbeute 66.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGwith stirring
  2. 2
    FiltrationThe precipitated crystals were filtered
  3. 3
    Sonstigerecrystallized

Vorschrift

Nε-Lauroyl-L-lysine (30 g) was dissolved in 0.2M aqueous NaOH solution (1 L), and ether was added. Adipic acid monoethyl ester acid chloride (26.4 g) was added to the ether layer, and the mixture was stirred at room temperature for 24 hr. To the aqueous solution was added hydrochloric acid with stirring, and the mixture was adjusted to about pH 1. The precipitated crystals were filtered and recrystallized to give Nε-lauroyl-Nα-(5-carboxypentanoyl)-L-lysine (27.42 g, yield 66%). 4.566 g thereof was dissolved in methanol (50 ml), 1M aqueous NaOH solution (10 ml) was added, and the mixture was stirred at room temperature for 3 hr. The solution was filtered, the solvent was removed, and the obtained solid was recrystallized. yield 4.7 g, 99%.

Quelle

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