Réaction #1889

ord-39af1e12beb24e17a8267182051aa7af

Équation de réaction

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
Rendement 95.7%
O=C(Nc1ccc(Cl)cc1C(O)c1ccccc1Cl)C(F)(F)F
5-chloro-α-(2-chlorophenyl)-2-(trifluoroacetylamino)benzyl alcohol
Rendement 95.7%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreAfter reaction
  2. 2
    Autrethe organic layer was dried
  3. 3
    Autreafter which the solvent was removed
  4. 4
    Autrethe residue was recrystallized from hexane

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05726306uspto-grants-1998_03