Réaction #170979

ord-33ed2fb4606d4f79b2c682cade20a772

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe catalyst was removed by filtration and ice water (2.5 L)
  2. 2
    workup.ADDITIONwas added to the filtrate
  3. 3
    FiltrationCrude 25 was filtered off
  4. 4
    Séchagedried and recrystal-lised in a mixture of methanol:chloroform (1:1)

Mode opératoire

(4-Nitrophenoxy)-acetic acid-2-[2-(4-nitrophenoxy)-acetoxy]-ethyl ester 24 (100 g, 238 mmol) was dissolved in dry dimethyl formamide (500 ml) in a pressure vessel, palladium on carbon (5%, 22 g) was added, and the mixture stirred under an atom-sphere of hydrogen (4 kg) for 6 hours. The catalyst was removed by filtration and ice water (2.5 L) was added to the filtrate. Crude 25 was filtered off, dried and recrystal-lised in a mixture of methanol:chloroform (1:1) to give pure 25 (65 g, 78%) as a light brown shining powder with an m.p. between 124-125.8° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08846845B2uspto-grants-2014_09