Azobisisobutyronitrile → HCID 18521725, compound

HRID 1031971Notes

Reaction equation

HRID 1031971 reaction equation
[Br:1]N1C(=O)CCC1=O.[CH3:9][C:10]1[O:11][C:12]2[CH:18]=[C:17]([N+:19]([O-:21])=[O:20])[CH:16]=[CH:15][C:13]=2[CH:14]=1.N(C(C)(C)C#N)=NC(C)(C)C#N>C(Cl)(Cl)(Cl)Cl>[Br:1][CH2:9][C:10]1[O:11][C:12]2[CH:18]=[C:17]([N+:19]([O-:21])=[O:20])[CH:16]=[CH:15][C:13]=2[CH:14]=1

Participants

5

Procedure

N-Bromosuccinimide ("NBS") (1.11 g, 6.2 mmole) was added to a solution of 2-methyl-6-nitrobenzofuran (1.00 g, 5.65 mmole) and azobisisobutyronitrile (20 mg) in carbon tetrachloride and the mixture was heated at reflux temperature for 11/2 hours in the presence of a bright light. The solvent was then evaporated and the residue dissolved in methylene chloride, washed with water, dried (MgSO4), evaporated to dryness and purified by column chromatography on silica eluting with methylene chloride/hexane (7:3). The product-containing fractions were combined and evaporated to give the title compound, yield 1.43 g. 'H-N.m.r. clearly showed that the product contained 20% of 2-dibromomethyl-6-nitrobenzofuran, however, it was not considered necessary to remove this and the product was used directly without further purification.

Workup

  1. temperaturethe mixture was heated
  2. temperatureat reflux temperature for 11/2 hours in the presence of a bright light
  3. customThe solvent was then evaporated
  4. dissolutionthe residue dissolved in methylene chloride
  5. washwashed with water
  6. dry with materialdried (MgSO4)
  7. customevaporated to dryness
  8. custompurified by column chromatography on silica eluting with methylene chloride/hexane (7:3)
  9. customevaporated

Sources & evidence

ORD record
ord-2b4a203b7b774346b63ffc7822d4dd3b
Source dataset
uspto-grants-1990_09
Patent number
US04956382

Reaction notes

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