Reacción #4547

ord-097ce1f06049442d8b63f92135cc032e

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroto react for 8 hours at 110° C
  2. 2
    OtroAfter the reaction
  3. 3
    Filtraciónfilter the insoluble matter
  4. 4
    LavadoThe organic layer is then washed with 5% NaOH, water and saturated salt water
  5. 5
    Otrodried
  6. 6
    Otroevaporated
  7. 7
    Otroto remove the ether

Procedimiento

Add 5.75 g of 4-cyanophenol 10 g of 1 brom-6-methyl octane synthesized of available active amyl alcohol, 6.67 g of anhydrous potassium carbonate, 30 ml of N,N-dimethyl formamide into 100 ml four-mouth flask under nitrogen atmosphere, allow to react for 8 hours at 110° C. After the reaction, filter the insoluble matter, then extract ether. The organic layer is then washed with 5% NaOH, water and saturated salt water, then dried and evaporated to remove the ether. Then when the obtained oily matter is refined, 11.4 g of optical (s)-4-(6-methyloctyloxy)benzonitrile is obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04725688uspto-grants-1988_02