Reaktion #2307974

ord-61f461a9220641e7a5da668761446396

Reaktionsgleichung

CCOC(=O)CCCCCOCCOCCOCCOCCOCCOCCOCc1ccccc1
benzyl ether
CCOC(=O)CCCCCOCCOCCOCCOCCOCCOCCOCc1ccccc1
6-{2-[2-(2-{2-[2-(2-Benzyloxyethoxy)ethoxy]ethoxy}-ethoxy)-ethoxy]-ethoxy}-hexanoic acid ethyl ester
CCOC(=O)CCCCCOCCOCCOCCOCCOCCOCCO
compound 4
Ausbeute 79.0%
CCOC(=O)CCCCCOCCOCCOCCOCCOCCOCCO
6-{2-[2-(2-{2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}-ethoxy)-ethoxy]-ethoxy}-hexanoic acid ethyl ester
Ausbeute 79.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe reaction mixture was filtered through Celite 545
  2. 2
    Sonstigeto remove the catalyst
  3. 3
    Einengenthe filtrate was concentrated in vacuo

Vorschrift

Substantially monodispersed benzyl ether 3 (1.03 g, 2.0 mmol) was dissolved in 25 ml ethanol. To this solution was added 270 mg 10% Pd/C, and the mixture was placed under a hydrogen atmosphere and stirred for four hours, at which time TLC showed the complete disappearance of the starting material. The reaction mixture was filtered through Celite 545 to remove the catalyst, and the filtrate was concentrated in vacuo to yield the monodispersed compound 4 as a clear oil (0.67 g, 79%). FAB MS: m/e 425 (M+H), 447 (M+Na).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07368260B2uspto-grants-2008_05