Myristoyl chloride → N-[3(R,S)-Tetradecanoyloxytetradecanoyloxy]succinimide

HRID 255473

Reaktionsgleichung

Reaktionsgleichung von HRID 255473
[OH:1][CH:2]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[CH2:3][C:4]([O:6][N:7]1[C:11](=[O:12])[CH2:10][CH2:9][C:8]1=[O:13])=[O:5].[C:25](Cl)(=[O:39])[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH3:38]>N1C=CC=CC=1>[C:25]([O:1][CH:2]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[CH2:3][C:4]([O:6][N:7]1[C:8](=[O:13])[CH2:9][CH2:10][C:11]1=[O:12])=[O:5])(=[O:39])[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH3:38]

Komponenten

4

Versuchsvorschrift

To a solution of 5.6 g of N-[3(R,S)-hydroxytetradecanoyloxy]succinimide in 150 ml pyridine cooled to 0° are added 4.9 g of tetradecanoylchloride and the reaction mixture maintained at 4° for 12 hours. Excess reagent is destroyed with water, the mixture concentrated by evaporation and the residue chromatographed over silica gel (toluene/ethylacetate=95/5) to obtained the title compound as a syrup.

Aufarbeitung

  1. temperaturethe reaction mixture maintained at 4° for 12 hours
  2. customExcess reagent is destroyed with water
  3. concentrationthe mixture concentrated by evaporation
  4. customthe residue chromatographed over silica gel (toluene/ethylacetate=95/5)

Quellen und Nachweise

ORD-Eintrag
ord-e4f40f97f1e24bfd9a0aa2dbc2fa56c5
Quelldatensatz
uspto-grants-1987_10
Patentnummer
US04698331

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