Reacción #74501

ord-3270066dc9494738a1fed70eb9f13b4f

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted with EtOAc
  2. 2
    LavadoThe organic layer was washed with water
  3. 3
    Secadobrine, dried over anhydrous MgSO4
  4. 4
    Filtraciónfiltered
  5. 5
    Concentraciónconcentrated in vacuo
  6. 6
    OtroThe crude residue was purified by column chromatography (3-10% EtOAc/hexanes)

Procedimiento

To a solution of (3-bromonaphthalen-1-yl)methanol in DMF (100 mL) was added imidazole (6.4 g, 93 mmol), DMAP (0.57 g, 4.7 mmol), and TIPSCl (15 mL, 70 mmol). The resulting solution was stirred at room temperature for 12 h, diluted with a saturated ammonium chloride and extracted with EtOAc. The organic layer was washed with water then brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo. The crude residue was purified by column chromatography (3-10% EtOAc/hexanes) to yield the title compound (17.9 g, 96%) as a colorless oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08541380B2uspto-grants-2013_09