Réaction #2446083

ord-8db7f6189676475c8a82170d539aecd7

Équation de réaction

[BH4-].[Na+]
NaBH4
CC(O)CN
1-amino-2-propanol
O=C1CCCCC1
cyclohexanone
CC(O)CNC1CCCCC1
1-(cyclohexylamino)propan-2-ol

Solvants

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.STIRRINGThe reaction mixture was stirred at rt for 15 minutes
  2. 2
    Autrequenched with water
  3. 3
    FiltrationThe reaction mixture was filtered through a Celite® pad
  4. 4
    Concentrationthe filtrate was concentrated
  5. 5
    workup.DISSOLUTIONThe residue was dissolved in DCM
  6. 6
    Séchagedried over Na2SO4
  7. 7
    Filtrationfiltered
  8. 8
    Concentrationconcentrated

Mode opératoire

To a stirred solution of 1-amino-2-propanol (1.0 mL, 13.31 mmol) in ethanol (15 mL) was added cyclohexanone (1.9 g, 19.9 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 15 minutes and then NaBH4 (0.725 g, 19.17 mmol) was added. The reaction mixture was stirred at rt for 15 minutes and then quenched with water. The reaction mixture was filtered through a Celite® pad and the filtrate was concentrated. The residue was dissolved in DCM, dried over Na2SO4, filtered and concentrated to provide 1-(cyclohexylamino)propan-2-ol. Yield: 2.6 g (crude). 1H NMR (DMSO-d6) δ 4.39-4.36 (m, 1 H), 3.61-3.57 (m, 1 H), 2.47-2.30 (m, 3 H), 1.78-1.75 (m, 2 H), 1.66-1.63 (m, 2 H), 1.55-1.52 (m, 1 H), 1.23-1.12 (m, 3 H), 1.03-0.89 (m, 5 H). 1-(cyclohexylamino)propan-2-ol may also be prepared by following procedure of Example 1.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08685418B2uspto-grants-2014_04