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Hydrogen Peroxide → 1-(2-Nitrophenyl)-2-pyrroleacetic acid, ethyl ester

HRID 3567
Notes
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Reaction equation

HRID 3567 reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[N:10]1[CH:14]=[CH:13][CH:12]=[CH:11]1)([O-:3])=[O:2].I[CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18].OO>CS(C)=O.O>[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[N:10]1[CH:14]=[CH:13][CH:12]=[C:11]1[CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])([O-:3])=[O:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 784Hydrogen Peroxide2×HCID 12183Ethyl iodoacetate2×HCID 5206111-(2-Nitrophenyl)pyrrole

Product 1

HCID 861831311-(2-Nitrophenyl)-2-pyrroleacetic acid, ethyl esterYield 10.9%

Reagents, catalysts & solvents 2

HCID 679Dimethyl SulfoxideSolvent
HCID 962
Water
Solvent

Procedure

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.

Workup

  1. customat room temperature
  2. stirringthe mixture stirred at room temperature for 1 day
  3. extractionextracted with diethyl ether
  4. extractionThe organic extract
  5. washis washed with water, brine
  6. dry with materialdried (Na2SO4)
  7. customThe solvent is removed
  8. customthe residue (2.12 g) chromatographed on silica gel with ethyl acetate-hexane (1:4) as solvent

Sources & evidence

ORD record
ord-f70be6f27b64480db21f26322eb94066
Source dataset
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05733905

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes