Reacción #833223

ord-ab06ba2d4e3c4bfeb34f0767d9b4793e

Ecuación de reacción

O=Cc1c(Cl)cc([N+](=O)[O-])cc1Cl
2,6-dichloro-4-nitrobenzaldehyde
N=C(N)NN.O=C(O)O
Aminoguanidine hydrogen carbonate
Cl
hydrochloric acid
Cl.N=C(N)NN=Cc1c(Cl)cc([N+](=O)[O-])cc1Cl
(2,6-dichloro-4-nitrobenzylidene amino)-guanidine hydrochloride

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added
  2. 2
    Temperaturathe suspension heated
  3. 3
    Temperaturaunder reflux for 2.5 h
  4. 4
    TemperaturaThe reaction mixture was cooled

Procedimiento

Aminoguanidine hydrogen carbonate (0.96 g, 7.0 mmol) was added to a solution of concentrated hydrochloric acid (0.6 cm3) in water (2 cm3). After diluting the resulting solution with ethanol (20 cm3), 2,6-dichloro-4-nitrobenzaldehyde (1.53 g, 7.0 mmol) was added and the suspension heated under reflux for 2.5 h. The reaction mixture was cooled and diluted with diethyl ether to yield (2,6-dichloro-4-nitrobenzylidene amino)-guanidine hydrochloride as a yellow solid, mp 190° C. (dec).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04602041uspto-grants-1986_07