Réaction #470393

ord-1c3b2775836a47fb856c886abebc0ef0

Équation de réaction

CC(C)c1cccc(C(C)C)c1Nc1ccccc1[N+](=O)[O-]
2,6-diisopropyl-N-(2-nitrophenyl)aniline
[H][H]
hydrogen
CC(C)c1cccc(C(C)C)c1Nc1ccccc1N
desired product
Rendement 99.0%
CC(C)c1cccc(C(C)C)c1Nc1ccccc1N
N1-(2,6-diisopropylphenyl)benzene-1,2-diamine
Rendement 99.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationThe catalyst was filtered off through a Celite bed
  2. 2
    AutreThe solvent was evaporated
  3. 3
    AutreThe product was used for the next step without further purification

Mode opératoire

2,6-diisopropyl-N-(2-nitrophenyl)aniline (9.5 g, 32 mmol) and 10% palladium on carbon (0.4 g) were mixed with 150 ml of ethanol under nitrogen in a plastic coated hydrogenation vessel. The mixture was put on a par hydrogenator and reacted under 40 psi of hydrogen until there is no pressure drop. The catalyst was filtered off through a Celite bed. The solvent was evaporated. The product was used for the next step without further purification. 8.5 g of desired product was obtained.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08367223B2uspto-grants-2013_02