Reacción #428817

ord-c75fc2d63c674a13b2c16a843f41fd3e

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowere separated
  2. 2
    Extracciónaqueous layer extracted with EtOAc
  3. 3
    LavadoCombined organic layers were washed with brine
  4. 4
    Concentraciónconcentrated under reduced pressure
  5. 5
    OtroPurification by flash chromatography (10%-50% EtOAc-hexanes gradient)

Procedimiento

A mixture of THP-phenol 136 (0.72 g, 2.08 mmol), p-toluenesulfonic acid monohydrate (0.366 g) in THF:H2O (3:1, 20 mL) was stirred at room temperature for 3.5 hr. The reaction mixture was treated with aqueous NaHCO3-brine solution, layers were separated and aqueous layer extracted with EtOAc. Combined organic layers were washed with brine and concentrated under reduced pressure. Purification by flash chromatography (10%-50% EtOAc-hexanes gradient) gave 2,2,2-trifluoro-N-(4-(3-hydroxyphenyl)butyl)acetamide as a colorless oil, which was taken into the next step. Yield (0.438 g, 96%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08895782B2uspto-grants-2014_11