Réaction #64353

ord-c6958f3c3a024d06824a5c716ce2de4d

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe solvent was removed
  2. 2
    workup.DISTILLATIONby distillation
  3. 3
    Autrethe residue was purified by silica gel column chromatography (developing solution; AcOEt:n-hexane=1:1)
  4. 4
    Autrerecrystallized from a mixture of n-hexane and ethyl acetate

Mode opératoire

A mixture of 1.00 g of 6-nitro-2,2-dimethyl-2H-1-benzopyran-4-carboxylic acid, 0.44 g of 2,2,2-trifluoroethylamine, 0.97 g of 2,2'-dipyridyl disulfide, 1.16 g of triphenylphosphine, and 20 ml of dichloromethane was stirred at room temperature for 3 hours. The solvent was removed therefrom by distillation, and the residue was purified by silica gel column chromatography (developing solution; AcOEt:n-hexane=1:1) and then recrystallized from a mixture of n-hexane and ethyl acetate to obtain 0.98 g of N (2',2',2'-trifluoroethyl)-6-nitro-2,2-dimethyl-2H-1-benzopyran-4-carboxamide represented by formula shown below.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05412117uspto-grants-1995_05