反应 #2446084

ord-33bf0ff1cb054590bd6e40976ffcb724

反应方程式

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

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The organic layer was separated
  2. 2
    洗涤washed with water and brine
  3. 3
    干燥dried over Na2SO4
  4. 4
    过滤filtered
  5. 5
    浓缩concentrated
  6. 6
    其他The crude material was purified by chromatography on silica-gel (230-400 mesh)
  7. 7
    洗涤eluting with 5% MeOH/DCM

实验过程

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).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08685418B2uspto-grants-2014_04