反应 #1583847

ord-7878d13113e443cd9f33911ff8643462

反应方程式

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
收率 66.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGwith stirring
  2. 2
    过滤The precipitated crystals were filtered
  3. 3
    其他recrystallized

实验过程

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%.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09198846B2uspto-grants-2015_12