Reacción #502134

ord-990212db697f42be81d128f566c1ac2f

Ecuación de reacción

CO
methanol
[Cl-].[NH4+]
ammonium chloride
[CH3][Al]([CH3])[CH3]
trimethylaluminium
N#CCc1ccc(Cl)c(Cl)c1
3,4-dichlorophenylacetonitrile
Cl.N=C(N)Cc1ccc(Cl)c(Cl)c1
title compound
Cl.N=C(N)Cc1ccc(Cl)c(Cl)c1
2-(3,4-Dichlorophenyl)ethanamidine hydrochloride

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe mixture is warmed to room temperature
  2. 2
    workup.STIRRINGthe mixture is stirred at 80° C. overnight
  3. 3
    TemperaturaAfter cooling to 0° C.
  4. 4
    OtroThe product is separated from the precipitated solid by filtration with suction
  5. 5
    Lavadothe filter cake is washed several times with methanol
  6. 6
    OtroThe combined filtrates are evaporated to dryness
  7. 7
    Filtraciónagain filtered with suction

Procedimiento

2.88 g (54 mmol) of ammonium chloride are suspended in 50 ml of toluene under an argon atmosphere and cooled to 0° C. After dropwise addition of 27 ml of a 2 M trimethylaluminium solution in toluene, the mixture is warmed to room temperature and then stirred for 1.5 h. 5 g (27 mmol) of 3,4-dichlorophenylacetonitrile are added, and the mixture is stirred at 80° C. overnight. After cooling to 0° C., 50 ml of methanol are added dropwise. The product is separated from the precipitated solid by filtration with suction, and the filter cake is washed several times with methanol. The combined filtrates are evaporated to dryness, and the residue is then suspended in dichloromethane/methanol 10:1 and again filtered with suction. Concentration of the filtrate results in 6.2 g (77% of theory) of the title compound.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08088769B2uspto-grants-2012_01