Réaction #62534

ord-28693ca372ef4f7ba550b18e0dc78d51

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureunder reflux for 10 hours
  2. 2
    Autrerecrystallizing from heptane

Mode opératoire

The above crude product of 4-(1-methyl-heptyloxy)-4'-hydroxy-azobenzene (16.5 g) was heated with lauryl bromide (16 g) in ethanol in the presence of KOH (3.6 g) under reflux for 10 hours, followed by passing a toluene solution of the product through an alumina chromatographic column and recrystallizing from heptane to obtain 4'-dodecyloxy-4'-(1-methyl-heptyloxy)-azobenzene

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04761246uspto-grants-1988_08