Azobisisobutyronitrile → HCID 18521725, compound

HRID 345034Notes

Reaction equation

HRID 345034 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 11/2hours 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 11/2hours 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-68a11246474c4c2c91ad7e597f1e1fae
Source dataset
uspto-grants-1991_10
Patent number
US05055473

Reaction notes

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