Réaction #992716

ord-21d6ba9caca04c3f9bbb3f352b77d03a

Équation de réaction

COc1ccccc1
anisole
O=[N+]([O-])c1ccc2c(c1)Oc1ccc([N+](=O)[O-])cc1O2
2,7-dinitrodibenzodioxin
[H][H]
hydrogen
Nc1ccc2c(c1)Oc1ccc(N)cc1O2
2,7-diaminodibenzodioxin
Rendement 46.1%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe 10% palladium/carbon was removed by filtration
  2. 2
    workup.ADDITIONa precipitate containing the 10% palladium/carbon
  3. 3
    Filtrationwas collected by filtration
  4. 4
    Lavagethe precipitate was rinsed with THF
  5. 5
    ConcentrationThe rinsings were concentrated
  6. 6
    Autredried under reduced pressure

Mode opératoire

To a mixture of 1200 ml of anisole and 800 ml of THF were added 69.7 g (0.254 mole) of 2,7-dinitrodibenzodioxin and 22.2 g of 10% palladium/carbon and hydrogen gas was passed through the mixture with stirring at room temperature for 8 hours. The 10% palladium/carbon was removed by filtration, then a precipitate containing the 10% palladium/carbon was collected by filtration, and the precipitate was rinsed with THF. The rinsings were concentrated and dried under reduced pressure to give 25.0 g (0.117 mole, 46.0% yield) of 2,7-diaminodibenzodioxin. The product showed a purity of 98.1% (HPLC, 254 nm).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08012606B2uspto-grants-2011_09