Aluminium lithium hydride → 2-Amino-2-(3,4-difluorophenyl)ethanol

HRID 1167686Notes

Reaction equation

HRID 1167686 reaction equation
[H-].[H-].[H-].[H-].[Li+].[Al+3].C[O:8][C:9](=O)[CH:10]([NH2:19])[C:11]1[CH:16]=[CH:15][C:14]([F:17])=[C:13]([F:18])[CH:12]=1>C1COCC1>[NH2:19][CH:10]([C:11]1[CH:16]=[CH:15][C:14]([F:17])=[C:13]([F:18])[CH:12]=1)[CH2:9][OH:8]

Participants

4

Conditions

Temperature
0 °C

Procedure

To a well stirred suspension of LiAlH4 (4.7 g, 0.125 mol) in THF (120 mL) in a 3-necked round bottom flask fitted with a condenser and a dropping funnel, was added a solution of amino-(3,4-difluorophenyl)-acetic acid methyl ester (10.0 g, 0.05 mol) in THF (100 mL) dropwise at 0° C. The resulting greenish brown suspension was then heated to reflux for 2 h. The reaction mixture was cooled to 0° C. and then carefully quenched sequentially with 5 mL of water, 5 mL of 3N NaOH followed by 15 mL of water. The resulting suspension was filtered through 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-2-(3,4-difluorophenyl)-ethanol was obtained as a yellow glassy syrup (8.6 g, 99%) which was used in the next step without further purification.

Workup

  1. customfitted with a condenser and a dropping funnel
  2. temperatureThe resulting greenish brown suspension was then heated
  3. temperatureto reflux for 2 h
  4. customcarefully quenched sequentially with 5 mL of water, 5 mL of 3N NaOH
  5. filtrationThe resulting suspension was filtered through a fritted glass funnel
  6. additionTo the residue was added 100 mL Et2O
  7. temperaturethe suspension was heated
  8. temperatureto reflux for 20 min
  9. filtrationThe suspension was filtered
  10. dry with materialdried over MgSO4
  11. filtrationfiltered
  12. customthe solvent was removed in vacuo

Sources & evidence

ORD record
ord-23b3088995e5404bac6f2a4c166ebbda
Source dataset
uspto-grants-2003_09
Patent number
US06620815B1

Reaction notes

Loading…