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1,3-Diiodo-5-nitrobenzene → 3,5-DIIODOANILINE

HRID 486835
Notes
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Reaction equation

HRID 486835 reaction equation
[I:1][C:2]1[CH:3]=[C:4]([N+:9]([O-])=O)[CH:5]=[C:6]([I:8])[CH:7]=1>C(O)C>[I:1][C:2]1[CH:3]=[C:4]([CH:5]=[C:6]([I:8])[CH:7]=1)[NH2:9]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 121342561,3-Diiodo-5-nitrobenzene

Product 1

HCID 121342543,5-DIIODOANILINEYield 61.9%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A mixture of 61.5 g (0.164M) of 3,5-diiodonitrobenzene and 111.1 g (0.4924M) of stannous chloride in 900 mL of ethanol was heated to reflux 1.5 hrs under nitrogen. The reaction mixture was cooled and most of the solvent was removed in vacuo. The residue was partitioned between ethyl acetate and excess ice-cold 5N sodium hydroxide and ice. The organic phase was separated, washed with sat'd sodium chloride solution, and dried over anhyd. magnesium sulfate. Solvent removal afforded a crude oil which was purified on silica gel using 8:1:1 mixture of hexane:methylene chloride:ethyl acetate to give 35 g of 3,5-diiodoaniline as a light tan colored solid.

Workup

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
temperature
was heated
  • temperatureto reflux 1.5 hrs under nitrogen
  • temperatureThe reaction mixture was cooled and most of the solvent
  • customwas removed in vacuo
  • customThe residue was partitioned between ethyl acetate and excess ice-cold 5N sodium hydroxide and ice
  • customThe organic phase was separated
  • washwashed with sat'd sodium chloride solution
  • customdried over anhyd
  • customSolvent removal
  • customafforded a crude oil which
  • customwas purified on silica gel using 8:1:1 mixture of hexane
  • Sources & evidence

    ORD record
    ord-410acc0ad4a048879d6105580d543ac9
    Source dataset
    uspto-grants-1994_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05292879

    Reaction notes

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