DL-beta-Phenylalanine → 1-Propanol, 3-amino-3-phenyl-

HRID 1167690Notes

Reaction equation

HRID 1167690 reaction equation
[H-].[H-].[H-].[H-].[Li+].[Al+3].[NH2:7][CH:8]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[CH2:9][C:10](O)=[O:11]>C1COCC1>[NH2:7][CH:8]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[CH2:9][CH2:10][OH:11]

Participants

4

Conditions

Temperature
0 °C

Procedure

To a well stirred suspension of LiAlH4 (1.3 g, 35.0 mmol) in THF (75 mL) in a round bottom flask fitted with a condenser was added 3-amino-3-phenyl-propionic acid (2.5 g, 15.0 mmol) in small portions at 0° C. The resulting grey suspension was then heated to reflux for 2 h. The reaction mixture was cooled to 0° C. and then carefully quenched sequentially with 1.3 mL of water, 1.3 mL of 3N NaOH followed by 4.0 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. 3-amino-3-phenyl-propan-1-ol was obtained as a white solid (2.30 g, 100%) which was used in the next step without further purification.

Workup

  1. customfitted with a condenser
  2. temperatureThe resulting grey suspension was then heated
  3. temperatureto reflux for 2 h
  4. customcarefully quenched sequentially with 1.3 mL of water, 1.3 mL of 3N NaOH
  5. filtrationThe resulting suspension was filtered thro' 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-dff7177ac97d4e63b125bd89c1c15769
Source dataset
uspto-grants-2003_09
Patent number
US06620815B1

Reaction notes

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