Reaktion #725925

ord-5fb8da9c07794063854d76ec989debf4

Reaktionsgleichung

CC(Oc1ccc([N+](=O)[O-])cc1)C(=O)OCCOC(=O)COc1ccc([N+](=O)[O-])cc1
2-(4-nitrophenoxy)propionic acid-2-[2-(4-nitrophenoxy)acetoxy]ethyl ester
CC(Oc1ccc([N+](=O)[O-])cc1)C(=O)OCCOC(=O)COc1ccc([N+](=O)[O-])cc1
2-(4-Nitro-phenoxy)-propionic acid 2-[2-(4-nitro-phenoxy)-acetoxy]-ethyl ester
CC(Oc1ccc(N)cc1)C(=O)OCCOC(=O)COc1ccc(N)cc1
56
Ausbeute 58.0%
CC(Oc1ccc(N)cc1)C(=O)OCCOC(=O)COc1ccc(N)cc1
2-(4-Aminophenoxy)propionic acid-2-[2-(4-aminophenoxy)acetoxy]ethyl ester
Ausbeute 58.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe catalyst was removed by filtration and ice water (1 L)
  2. 2
    workup.ADDITIONwas added to the filtrate
  3. 3
    ExtraktionCrude 56 was extracted into ethyl acetate
  4. 4
    Trocknendried over Na2SO4
  5. 5
    workup.DISTILLATIONdistilled
  6. 6
    Sonstigepurified by column chromatography on silica gel

Vorschrift

2-(4-nitrophenoxy)propionic acid-2-[2-(4-nitrophenoxy)acetoxy]ethyl ester 55 (20 g, 50 mmol) was dissolved in dry dimethylformamide (150 ml) in a pressure vessel, palladium on carbon (5%, 5 g) added, and the mixture stirred under a hydrogen atm. (4 Kg) for 3 hrs. The catalyst was removed by filtration and ice water (1 L) was added to the filtrate. Crude 56 was extracted into ethyl acetate, dried over Na2SO4, distilled and purified by column chromatography on silica gel using chloroform:ethyl acetate (8:2) to give pure 56 (10 g, 58%) as a dark brown syrup.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07691364B2uspto-grants-2010_04