Reacción #424440

ord-266f456e38fa4eac88f404e48577250d

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadowashed with water (20 ml) and brine
  2. 2
    SecadoThe organic layer was dried over Na2SO4
  3. 3
    Filtraciónfiltered
  4. 4
    Concentraciónconcentrated
  5. 5
    Otropurified by flash chromatography on a silica gel column (hex: ethyl acetate 2:1)

Procedimiento

To a stirred solution of 2-(3-Hydroxy-4-methylphenyl)acetonitrile (Step A, 2.18 g, 14.8 mmol), K2CO3 (2.66 g, 19.2 mmol) in dry DMF (20 ml) was added 2,6-Dimethylbenzyl chloride (2.97 g, 19.2 mmol) at room temperature under argon. The reaction mixture was stirred for 16 hours, diluted with EtOAc (40 ml), washed with water (20 ml) and brine. The organic layer was dried over Na2SO4, filtered, concentrated, and purified by flash chromatography on a silica gel column (hex: ethyl acetate 2:1) to give the title compound as a white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08889724B2uspto-grants-2014_11