Реакция #1889

ord-39af1e12beb24e17a8267182051aa7af

Уравнение реакции

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

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеAfter reaction
  2. 2
    Другоеthe organic layer was dried
  3. 3
    Другоеafter which the solvent was removed
  4. 4
    Другоеthe residue was recrystallized from hexane

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05726306uspto-grants-1998_03