Reacción #1889

ord-39af1e12beb24e17a8267182051aa7af

Ecuación de reacción

Nc1ccc(Cl)cc1C(O)c1ccccc1Cl
2-amino-5-chloro-α-(2-chlorophenyl)benzyl alcohol
O=C(O)C(F)(F)F
trifluoroacetic acid
O=C([O-])O.[Na+]
sodium hydrogen carbonate
O=C(Nc1ccc(Cl)cc1C(O)c1ccccc1Cl)C(F)(F)F
crystal
Rendimiento 95.7%
O=C(Nc1ccc(Cl)cc1C(O)c1ccccc1Cl)C(F)(F)F
5-chloro-α-(2-chlorophenyl)-2-(trifluoroacetylamino)benzyl alcohol
Rendimiento 95.7%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroAfter reaction
  2. 2
    Otrothe organic layer was dried
  3. 3
    Otroafter which the solvent was removed
  4. 4
    Otrothe residue was recrystallized from hexane

Procedimiento

To a solution of 1.0 g of 2-amino-5-chloro-α-(2-chlorophenyl)benzyl alcohol in 12 ml of dichloromethane, a solution of 0.8 g of anhydrous trifluoroacetic acid in 2 ml of dichloromethane was added. After reaction, an aqueous solution of sodium hydrogen carbonate was added, and the organic layer was dried, after which the solvent was removed and the residue was recrystallized from hexane to yield 1.3 g of a crystal.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05726306uspto-grants-1998_03