Reacción #674297

ord-1ad501c69fca4463955e913e872b85ab

Ecuación de reacción

CB1OC(c2ccccc2)(c2ccccc2)[C@H]2CCCN12
(R)-2-methyl-CBS-oxazaborolidine
CSC
Me2S
ClCCl
dichloromethane
CC(=O)c1c(Cl)ccc(F)c1Cl
1-(2,6-dichloro-3-fluorophenyl)ethanone
C[C@H](O)c1c(Cl)ccc(F)c1Cl
(S)-1-(2,6-dichloro-3-fluorophenyl)ethanol

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONis added
  2. 2
    Filtraciónthe resulting mixture is filtered through a pad of celite and silica gel
  3. 3
    Lavadowashed with 30% EtOAc in hexane
  4. 4
    OtroThe solvent is removed under reduced pressure
  5. 5
    Otrothe resulting oil is purified by flash chromatography (20% EtOAc in hexane)

Procedimiento

To (R)-2-methyl-CBS-oxazaborolidine (Aldrich or Callery Chemical Co, 1M in toluene, 1 eq.) at −45° C. is added BH3. Me2S (1.06 eq.). To the previous solution is added at −30° C. a 1M dichloromethane solution of 1-(2,6-dichloro-3-fluorophenyl)ethanone. After completion of the reaction, excess MeOH is added followed by IN HCl. After warming up to room temperature, the resulting mixture is filtered through a pad of celite and silica gel and washed with 30% EtOAc in hexane. The solvent is removed under reduced pressure and the resulting oil is purified by flash chromatography (20% EtOAc in hexane) to afford (S)-1-(2,6-dichloro-3-fluorophenyl)ethanol (optically enriched).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09226923B2uspto-grants-2016_01