Reacción #80036

ord-812690fa45fb48b6954987b2bea6885d

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted with EtOAc
  2. 2
    LavadoThe combined organic layers were washed with H2O and saturated aqueous NaCl
  3. 3
    Secadobefore being dried (MgSO4)
  4. 4
    Concentraciónconcentrated under reduced pressure

Procedimiento

To a solution of 4-bromo-3-tert-butylphenol (Intermediate 104, 1.17 g, 5.10 mmols) and imidazole (520.0 mg, 7.65 mmols) in 10 mL DMF was added chloro-triisopropylsilane (1.18 g, 6.10 mmols). After stirring overnight at room temperature the solution was diluted wirth H2O and extracted with EtOAc. The combined organic layers were washed with H2O and saturated aqueous NaCl before being dried (MgSO4) and concentrated under reduced pressure. The title compound, 1.80 g (92%), was isolated by column chromatography (0-1.5% EtOAc-hexanes) as a colorless oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06713647B2uspto-grants-2004_03