Reacción #5705

ord-60b3074aefe344eab4ea2ade849112af

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe cooling bath was removed
  2. 2
    workup.ADDITIONafter addition
  3. 3
    OtroThe precipitated white solid was collected
  4. 4
    Lavadowashed with ether-hexane (1:1)
  5. 5
    Otrorecrystallized from acetone-ethyl acetate-ether solvent mixture

Procedimiento

A magnetically stirred solution of methyl α-[3-(trifluoromethyl)benzylamino]-1-benzylindole-3-acetate (4.07 g, 9.0 mmol) in 65 mL of ether cooled at 0°-5° C. was treated dropwise over a four-minute period with a stock solution of hydrogen chloride in ether (3.8 mL, 11.71 mmol, 1.3 eq, 3.1 mmol per mL). The cooling bath was removed after addition was completed and the mixture stirred at room temperature overnight. The precipitated white solid was collected, washed with ether-hexane (1:1) and recrystallized from acetone-ethyl acetate-ether solvent mixture to yield 4.18 g (95%) of the title compound.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05245046uspto-grants-1993_09