Reacción #10861

ord-7c8877349ecd41a09bb37cf0c4de17f1

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted (dichloromethane)
  2. 2
    Lavadowashed (water)
  3. 3
    Secadodried (magnesium sulfate)
  4. 4
    Otroevaporated
  5. 5
    Otroto give a mixture which

Procedimiento

2-(2,6-Dichloro-4-trifluoromethylphenylhydrazono) succinonitrile (0.296 g, 1 mmol), sodium cyanide (0.196 g, 4 equivalents), water (1 ml) and acetic acid (5 ml) were added successively to a sealed tube. After reacting for 40 hours at 20° C., the mixture was added to saturated sodium bicarbonate solution, extracted (dichloromethane), washed (water), dried (magnesium sulfate) and evaporated to give a mixture which contained 40% of the desired title compound, NMR 3.1 (m, 2H), 4.5 (m, 1H), 5.89 (m, 1H), 6.94 (d, 1H), 7.71 (s, 2H), together with 60% of unchanged starting hydrazone.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07094906B2uspto-grants-2006_08