Diethyl Ether → 2-Amino-1-(3,4-difluorophenyl)ethan-1-ol

HRID 1275200Notes

Reaction equation

HRID 1275200 reaction equation
[OH:1][CH:2]([C:5]1[CH:10]=[CH:9][C:8]([F:11])=[C:7]([F:12])[CH:6]=1)[C:3]#[N:4].[H-].[H-].[H-].[H-].[Li+].[Al+3].CCOCC>>[NH2:4][CH2:3][CH:2]([C:5]1[CH:10]=[CH:9][C:8]([F:11])=[C:7]([F:12])[CH:6]=1)[OH:1]

Participants

4

Procedure

To a well stirred solution of hydroxy-(3,4-difluorophenyl)-acetonitrile (3.34 g, 20 mmol), was added a 1.0 M solution of LiAlH4 in ether (40 mL, 40 mmol) dropwise at 0° C. The resulting yellow solution was then stirred at room temperature for 2 h. The reaction mixture was cooled to 0° C. and then carefully quenched sequentially with 1.5 mL of water, 1.5 mL of 3N NaOH followed by 4.5 mL of water. The resulting suspension was filtered thro' a fritted glass funnel. To the residue was added 100 mL Et2O and the suspension was heated to reflux for 20 min. The suspension was filtered and was combined with the previous filtrate, dried over MgSO4, filtered and the solvent was removed in vacuo. 2-amino-1-(3,4-difluorophenyl)-ethanol was obtained as a yellow glassy syrup (3.3 g, 99%) which was used in the next step without further purification.

Workup

  1. temperatureThe reaction mixture was cooled to 0° C.
  2. customcarefully quenched sequentially with 1.5 mL of water, 1.5 mL of 3N NaOH
  3. filtrationThe resulting suspension was filtered thro' a fritted glass funnel
  4. additionTo the residue was added 100 mL Et2O
  5. temperaturethe suspension was heated
  6. temperatureto reflux for 20 min
  7. filtrationThe suspension was filtered
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. customthe solvent was removed in vacuo

Sources & evidence

ORD record
ord-4a951658d1d34bb1b86c4ece6a18973a
Source dataset
uspto-grants-2000_12
Patent number
US06159990

Reaction notes

Loading…