Réaction #568962

ord-e24f2e9a41da499cbe6e9b9bc8c23963

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONThe reaction mixture was poured into ice
  2. 2
    Extractionextracted with ethyl acetate
  3. 3
    LavageThe organic layer was washed with saturated aqueous solution of sodium chloride
  4. 4
    Séchagedried with anhydrous sodium sulfate
  5. 5
    AutreThe desiccant was separated by filtration
  6. 6
    Autrethe filtrate was purified by silica gel column chromatography

Mode opératoire

1.0 g of 1-methyl-3,4-dihydroisoquinoline was dissolved in 7.0 ml of conc. nitric acid at 0° C., and 14.0 ml of fuming nitric acid was added dropwise to the solution. The solution was stirred for one hour at the same temperature, and overnight at room temperature. The reaction mixture was poured into ice, neutralized with aqueous solution of sodium hydroxide, and extracted with ethyl acetate. The organic layer was washed with saturated aqueous solution of sodium chloride, and dried with anhydrous sodium sulfate. The desiccant was separated by filtration, and the filtrate was purified by silica gel column chromatography to obtain 1.08 g of 1-methyl-7-nitro-3,4-dihydroisoquinoline, which was white crystal (yield: 82%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05789595uspto-grants-1998_08