Reacción #998631

ord-14d2939c140f4b5e808ef25b54d4d027

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextract three times with EtOAc
  2. 2
    SecadoDry over anhydrous Na2SO4
  3. 3
    Concentraciónconcentrate in vacuo

Procedimiento

To 2,2-bis(trifluoromethyl)propanol (4.34 g, 22.1 mmol) in DCM (100 mL) at 0° C. add with stirring triethylamine (6.2 mL, 44 mmol) followed by methanesulfonyl chloride (2.6 mL, 33 mmol). After 15 min at 0° C. dilute with water and extract three times with EtOAc. Dry over anhydrous Na2SO4 and concentrate in vacuo to give the crude desired intermediate as a yellow oil (6.16 g, 100%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08022062B2uspto-grants-2011_09