Reacción #1880946

ord-cf545d6e40c44a138df70176955c79d2

Ecuación de reacción

N#Cc1ccc(N=Nc2ccc(OCCO)c(Br)c2)cc1
4-(2-hydroxyethyloxy)-3-bromo-4′-cyanoazobenzene
N#[C][Cu][C]#N
copper cyanide
N
ammonia
N#Cc1ccc(N=Nc2ccc(OCCO)c(C#N)c2)cc1
4-(2-Hydroxyethyloxy)-3,4′-dicyanoazobenzene

Disolventes

Condiciones de reacción

Temperatura
140°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónthe precipitate is filtered off
  2. 2
    workup.DISSOLUTIONThe precipitate is dissolved in hot dioxane
  3. 3
    FiltraciónThe solution is filtered off from the undissolved residue
  4. 4
    Otrothe dioxane is evaporated off on a rotary evaporator
  5. 5
    Otrothe product is purified by chromatography on silica gel in toluene/THF (½)
  6. 6
    Otrorecrystallized once from ethanol

Procedimiento

15 g (4-(2-hydroxyethyloxy)-3-bromo-4′-cyanoazobenzene are dissolved in 25 ml hot DMF. 4.3 g copper cyanide are then added and the reaction mixture is stirred at 140° C. for 5–6 hours. This solution is added to approx. 500 ml of a 13% aqueous ammonia solution and the precipitate is filtered off. The precipitate is dissolved in hot dioxane. The solution is filtered off from the undissolved residue, the dioxane is evaporated off on a rotary evaporator and the product is purified by chromatography on silica gel in toluene/THF (½) and recrystallized once from ethanol. The yield of 4-(2-hydroxyethyloxy)-3,4′-dicyanoazobenzene is 4.5 g. M.p.=138° C.; max=356 nm (DMF).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07022460B2uspto-grants-2006_04