Reaktion #434957

ord-a3b5ea743c93421498bfa61a758e502b

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction was quenched with MeOH (5 mL), volatiles
  2. 2
    Sonstigewere evaporated
  3. 3
    Sonstigethe residue was partitioned between water and EtOAc
  4. 4
    WaschenThe organic layer was washed with saturated NaHCO3/water, brine
  5. 5
    Trocknendried (sodium sulfate)
  6. 6
    Sonstigeevaporated

Vorschrift

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).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07176211B2uspto-grants-2007_02