Reacción #56778

ord-2e5d3a502d464a9f913b30a437bfa2a0

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction was quenched with MeOH (5 mL), volatiles
  2. 2
    Otrowere evaporated
  3. 3
    Otrothe residue was partitioned between water and EtOAc
  4. 4
    LavadoThe organic layer was washed with saturated NaHCO3/water, brine
  5. 5
    Secadodried (sodium sulfate)
  6. 6
    Otroevaporated

Procedimiento

A solution of N-(t-butyloxycarbonyl)cyclohexylglycine (2.0 g, 7.77 mmol) in anhydrous THF (10 mL) was cooled to 0° C. Borane solution (1 M in THF, 15.5 mL, 15.5 mmol) was added slowly and the reaction mixture was warmed to room temperature and stirred for 2 hours. The reaction was quenched with MeOH (5 mL), volatiles were evaporated and the residue was partitioned between water and EtOAc. The organic layer was washed with saturated NaHCO3/water, brine, dried (sodium sulfate), and evaporated to give tert-butyl 1-cyclohexyl-2-hydroxyethylcarbamate 4a (1.26 g, 66.7%), MS (CI) m/z 144.2 (MH+-Boc).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07419983B2uspto-grants-2008_09