Reaktion #3663

ord-f70be6f27b64480db21f26322eb94066

Reaktionsgleichung

OO
hydrogen peroxide
CCOC(=O)CI
ethyl iodoacetate
OO
hydrogen peroxide
O=[N+]([O-])c1ccccc1-n1cccc1
1-(2-nitrophenyl)pyrrole
CCOC(=O)CI
ethyl iodoacetate
CCOC(=O)Cc1cccn1-c1ccccc1[N+](=O)[O-]
product
Ausbeute 10.9%
CCOC(=O)Cc1cccn1-c1ccccc1[N+](=O)[O-]
1-(2-Nitrophenyl)-2-pyrroleacetic acid, ethyl ester
Ausbeute 10.9%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeat room temperature
  2. 2
    workup.STIRRINGthe mixture stirred at room temperature for 1 day
  3. 3
    Extraktionextracted with diethyl ether
  4. 4
    ExtraktionThe organic extract
  5. 5
    Waschenis washed with water, brine
  6. 6
    Trocknendried (Na2SO4)
  7. 7
    SonstigeThe solvent is removed
  8. 8
    Sonstigethe residue (2.12 g) chromatographed on silica gel with ethyl acetate-hexane (1:4) as solvent

Vorschrift

To a stirred mixture of 1.88 g of 1-(2-nitrophenyl)pyrrole, 4.80 g of ethyl iodoacetate and 2.22 g of FeSO4.7H2O in 40 ml of dimethyl sulfoxide is added dropwise 10 ml of 30% hydrogen peroxide while keeping the reaction mixture at room temperature with a cold water bath. The mixture is stirred at room temperature for one day. An additional 2.4 g of ethyl iodoacetate, 1.1 g of FeSO4.7H2O and 5 ml of 30% hydrogen peroxide is added and the mixture stirred at room temperature for 1 day. The mixture is diluted with water and extracted with diethyl ether. The organic extract is washed with water, brine and dried (Na2SO4). The solvent is removed and the residue (2.12 g) chromatographed on silica gel with ethyl acetate-hexane (1:4) as solvent to give 0.30 g of product as a brown gum.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05733905uspto-grants-1998_03