Reacción #82742

ord-d8ec55e141424ed1a7ead9eed3a444d6

Reactivos

Ninguno

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    workup.STIRRINGthe reaction mixture was kept stirring at room temperature for 18 h
  3. 3
    OtroThen a solution with white precipitates
  4. 4
    Otroformed
  5. 5
    Otrothe precipitates were removed by filtration
  6. 6
    LavadoThe etherate solution was washed with aqueous HCl (1N, 30 mL, two times) as well as brine
  7. 7
    Secadodried over MgSO4
  8. 8
    Filtraciónfiltered
  9. 9
    Concentraciónconcentrated
  10. 10
    Otrodried under vacuum

Procedimiento

A solution of cyanogen bromide (1.59 g, 15 mmol) in diethylether (20) was added dropwise to a solution of 4-isopropylaniline (3.24 g) in diethylether (50 mL) at 4° C. with stirring. After the addition, the reaction mixture was kept stirring at room temperature for 18 h. Then a solution with white precipitates formed and the precipitates were removed by filtration. The etherate solution was washed with aqueous HCl (1N, 30 mL, two times) as well as brine, dried over MgSO4, filtered, concentrated, and dried under vacuum to yield 4-isopropylphenyl cyanamide (2.0 g, 84%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05622968uspto-grants-1997_04