반응 #2446084

ord-33bf0ff1cb054590bd6e40976ffcb724

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The organic layer was separated
  2. 2
    세척washed with water and brine
  3. 3
    건조dried over Na2SO4
  4. 4
    여과filtered
  5. 5
    농축concentrated
  6. 6
    기타The crude material was purified by chromatography on silica-gel (230-400 mesh)
  7. 7
    세척eluting with 5% MeOH/DCM

실험 절차

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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08685418B2uspto-grants-2014_04