Reacción #76333

ord-73ca825ebf214663a74506c9c8a9a65f

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted with Et2O
  2. 2
    LavadoThe organic layer was washed with 2.5 N NaOH, 1 N HCl, saturated NaHCO3 and brine
  3. 3
    Secadodried (MgSO4)
  4. 4
    Otroevaporated

Procedimiento

Ex-605A) A slurry of 3-hydroxybenzaldehyde (1.22 g, 10 mmol), 2-chloropyrimidine (1.14 g, 10 mmol) and K2CO3 (1.65 g, 12 mmol) in DMSO (20 mL) was heated to 100° C. for 1 h. The cooled mixture was poured into water and extracted with Et2O. The organic layer was washed with 2.5 N NaOH, 1 N HCl, saturated NaHCO3 and brine, dried (MgSO4) and evaporated to yield 1.42 g (71%) of the desired 3-(2-pyrimidinyl-oxy)benzaldehyde product as a white solid which was used without further purification. 1H NMR (C6D6) δ7.12 (t, 1H), 7.54 (m, 1H), 7.66 (t, 1H), 7.78 (m, 1H), 7.83 (m, 1H), 8.64 (d, 2H), 10.05 (s, 1H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06699898B2uspto-grants-2004_03