Réaction #2204014

ord-096ab35058324866a92f3178e96efdfd

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe mixture was reacted at room temperature for 1 hr
  2. 2
    AutreThe organic layer was dried
  3. 3
    Concentrationconcentrated
  4. 4
    AutreThe obtained oily substance was purified by silica gel column chromatography

Mode opératoire

To a solution of N-[2-(2,3,4,5-tetramethylcyclopentadienyl)phenylmethylene]-N-(2,6-diisopropylphenyl)amine (10.0 mmol) in acetic acid (7.0 mL) was added sodium borohydride (13.0 mmol). The mixture was reacted at room temperature for 1 hr. Water and toluene were then added to the reaction mixture. The organic layer was dried and concentrated. The obtained oily substance was purified by silica gel column chromatography to give N-[2-(2,3,4,5-tetramethylcyclopentadienyl)phenylmethyl]-N-(2,6-diisopropylphenyl)amine (3.19 g, yield 82.4%) as a yellow oily substance.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07439379B2uspto-grants-2008_10