Reacción #1857543

ord-f381336cc96d4fc8ae01156e6b15ff59

Ecuación de reacción

CC1(c2ccc(Oc3ccc(Cl)cc3)cc2Cl)CO1
2-[2-chloro-4-(4-chlorophenoxy)phenyl]-2-methyloxirane
c1nc[nH]n1
1,2,4-triazole
[Na+].[OH-]
sodium hydroxide
CC(O)(Cn1cncn1)c1ccc(Oc2ccc(Cl)cc2)cc1Cl
2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1,2,4-triazol-1-yl)propan-2-ol

Disolventes

Condiciones de reacción

Temperatura
110°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction mixture was then partitioned between MTBE and aq. NaHCO3 solution
  2. 2
    Extracciónthe aq. phase was extracted twice with MTBE
  3. 3
    LavadoThe combined organic phases were washed with water (2×)
  4. 4
    Otrodried
  5. 5
    Otroevaporated
  6. 6
    OtroThe crude product was crystallized from diisopropyl ether

Procedimiento

A mixture of 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-2-methyloxirane (109 g), 1,2,4-triazole (27 g) and sodium hydroxide (16 g) in NMP (1 L) was heated to 110° C. for 1 h. The reaction mixture was then partitioned between MTBE and aq. NaHCO3 solution and the aq. phase was extracted twice with MTBE. The combined organic phases were washed with water (2×), dried and evaporated. The crude product was crystallized from diisopropyl ether.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09247746B2uspto-grants-2016_02