Reaction #2446084

ord-33bf0ff1cb054590bd6e40976ffcb724

Reaction equation

CC(O)CNC1CCCCC1
1-(cyclohexylamino)-propan-2-ol
C=O
HCHO
CC(=O)O[BH-](OC(C)=O)OC(C)=O.[Na+]
Na(OAc)3BH
CC(=O)O
acetic acid
CC(O)CN(C)C1CCCCC1
1-(cyclohexyl(methyl)amino)propan-2-ol

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherThe organic layer was separated
  2. 2
    Washwashed with water and brine
  3. 3
    Dryingdried over Na2SO4
  4. 4
    Filtrationfiltered
  5. 5
    Concentrationconcentrated
  6. 6
    OtherThe crude material was purified by chromatography on silica-gel (230-400 mesh)
  7. 7
    Washeluting with 5% MeOH/DCM

Procedure

To a stirred solution of 1-(cyclohexylamino)-propan-2-ol (crude 2.6 g) in DCE (30 mL) were added successively HCHO (35% in water, 2.1 mL, 24.8 mmol), Na(OAc)3BH (10.5 g, 49.6 mmol) and acetic acid (1 mL) at ice-cold conditions. The resulting mixture was allowed to stir at rt for 16 hours. The reaction was diluted with ethyl acetate and basified with 1N NaOH. The organic layer was separated, washed with water and brine, dried over Na2SO4, filtered and concentrated. The crude material was purified by chromatography on silica-gel (230-400 mesh) eluting with 5% MeOH/DCM to provide 1-(cyclohexyl(methyl)amino)propan-2-ol. Yield: 1.0 g 1H NMR (DMSO-d6) δ 4.11 (brs, 1 H), 3.65-3.57 (m, 1 H), 2.35-2.20 (m, 3 H), 2.19 (s, 3 H), 1.72-1.68 (m, 4 H), 1.57-1.54 (m, 1 H), 1.24-1.05 (m, 5 H), 1.01 (d, J=6 Hz, 3 H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08685418B2uspto-grants-2014_04