Reacción #1551173

ord-cd08060c5a034259aca58f73dbb16c0c

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction mixture was evaporated in vacuo
  2. 2
    workup.ADDITIONTo the residue was added diethyl ether (400 ml)
  3. 3
    Filtraciónthe resultant precipitate was filtered off
  4. 4
    workup.ADDITIONa mixture of ethyl acetate and hexane (2:3) as an eluent
  5. 5
    workup.ADDITIONFractions containing the object compound
  6. 6
    Otroevaporated

Procedimiento

To a solution of hydrazinoacetaldehyde diethyl acetal (52.6 g) in ethanol (110 ml) was added dropwise a solution of ethoxymethylenemalononitrile (41.5 g) in ethanol (420 ml) at room temperature. The mixture was stirred at ambient temperature for 24 hours. The reaction mixture was evaporated in vacuo. To the residue was added diethyl ether (400 ml) and the resultant precipitate was filtered off. The filtrate was subjected to column chromatography on silica gel using a mixture of ethyl acetate and hexane (2:3) as an eluent. Fractions containing the object compound were combined and evaporated to give 5-amino-4-cyano-1-(2,2-diethoxyethyl)pyrazole (23.0 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05302712uspto-grants-1994_04