Reacción #164147

ord-0ad078fcfe7a4e599117c5c8a2647570

Disolventes

Condiciones de reacción

Temperatura
120°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe resulting crude is partitioned between EtOAc (200 mL) and 1N HCl (200 mL)
  2. 2
    Extracciónthe aqueous phase is extracted with EtOAc (3×200 mL)
  3. 3
    SecadoThe combined organic layers are dried over Na2SO4
  4. 4
    Filtraciónfiltered
  5. 5
    Otroevaporated under vacuum

Procedimiento

Aniline (16.8 mL, 184 mmol) is added to a solution of (S)-methyl 2-(methylsulfonyloxy)-2-phenylacetate (I5) (22.4 g, 92.0 mmol) in CH3CN (50 mL). The mixture is heated under MW irradiation at 120° C. for 5 minutes (UPLC-MS monitoring: complete conversion). The resulting crude is partitioned between EtOAc (200 mL) and 1N HCl (200 mL) and the aqueous phase is extracted with EtOAc (3×200 mL). The combined organic layers are dried over Na2SO4, filtered and evaporated under vacuum to obtain 20.3 g of a pale yellow solid (92% yield), which is used in the next step without any additional purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08835682B2uspto-grants-2014_09