Reacción #55648

ord-0382624145fe452ebdea526e51f67c5a

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONis added
  2. 2
    OtroThe glyme is evaporated in vacuo
  3. 3
    workup.ADDITIONthe residue is mixed with 10% hydrochloric acid (200 ml)
  4. 4
    Temperaturarefluxed for 6.0 hours
  5. 5
    TemperaturaAfter cooling
  6. 6
    Extracciónthe mixture is extracted with ethyl acetate
  7. 7
    ExtracciónThe ethyl acetate extract
  8. 8
    Lavadois washed once with brine
  9. 9
    Otrodried
  10. 10
    Otroevaporated
  11. 11
    Lavadofor elution

Procedimiento

To a solution of cyanoacetic acid (3.57 g), in water (20 ml) is added a solution of sodium hydroxide (2.08 g) in water (20 ml). The solution is diluted with glyme (70 ml), 4-methoxyphenyl acetaldehyde (3.0 g) is added and the mixture is left at room temperature for 6.0 hours. The glyme is evaporated in vacuo, and the residue is mixed with 10% hydrochloric acid (200 ml) and refluxed for 6.0 hours. After cooling, the mixture is extracted with ethyl acetate. The ethyl acetate extract is washed once with brine, dried, evaporated and the residue subjected to chromatography on a column of silica gel using chloroform-ethyl acetate mixtures for elution to afford 2.2 g of 3-[(4-methoxyphenyl)methyl]glutaric acid. Crystallization from a benzene-ethyl acetate-hexane mixture gives a specimen having a melting point 109°-110° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04221725uspto-grants-1980_09