Reaktion #4855

ord-52be2b750bf64c28aee0f8bfed4840c7

Reaktionsgleichung

CC1Cc2cc([N+](=O)[O-])cc([N+](=O)[O-])c2O1
2,3-dihydro-5,7-dinitro-2-methyl-benzofuran
CN
methylamine
CNc1c(CC(C)O)cc([N+](=O)[O-])cc1[N+](=O)[O-]
1-(2-methylamino-3,5-dinitrophenyl)-2-propanol

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturAfter the mixture is cooled
  2. 2
    Sonstigethe expected product precipitates
  3. 3
    Waschenwashed with alcohol
  4. 4
    Sonstigerecrystallized from 50 ml of 96° strength ethanol
  5. 5
    SonstigeAfter being dried
  6. 6
    Sonstige0.047 mole (12 g) is obtained of a product which melts at 132° C.

Vorschrift

0.056 Mole (12.5 g) of 2,3-dihydro-5,7-dinitro-2-methyl-benzofuran is suspended in 100 ml of a 33% strength solution of methylamine in ethanol. After 10 hours' stirring at room temperature in a sealed Erlenmeyer, the reaction mixture is brought for 30 minutes to the refluxing temperature of the alcohol. After the mixture is cooled, the expected product precipitates. It is drained, washed with alcohol and then recrystallized from 50 ml of 96° strength ethanol. After being dried, 0.047 mole (12 g) is obtained of a product which melts at 132° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04727192uspto-grants-1988_02