Hydrochloric Acid → 1-Phenylethanol, (S)-

HRID 842338Notes

Reaction equation

HRID 842338 reaction equation
[OH-].[K+].[C:3]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)(=[O:5])[CH3:4].Cl>CC(O)C>[C:6]1([C@@H:3]([OH:5])[CH3:4])[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1

Participants

5

Conditions

Temperature
60 °C

Procedure

To the catalyst solution was added a degassed 0.1M solution of KOH in 2-propanol, followed by a solution of acetophenone in 2-propanol. The mixture was warmed to 60° C. and stirred at ambient temperature under nitrogen for 1 h, then worked up by neutralising with dilute hydrochloric acid and concentrating by vacuum distillation. The residue was diluted with ethyl acetate and washed with an equal volume of saturated aqueous sodium chloride. The organic layer was separated, dried over magnesium sulphate, separated from the solid and freed of solvent to give crude (S)-1-phenylethanol (0.9 g). Yield 43%, ee 80%. The turnover number, integrated over 1 h, was 410 h−1.

Workup

  1. concentrationconcentrating by vacuum distillation
  2. additionThe residue was diluted with ethyl acetate
  3. washwashed with an equal volume of saturated aqueous sodium chloride
  4. customThe organic layer was separated
  5. dry with materialdried over magnesium sulphate
  6. customseparated from the solid and freed of solvent

Sources & evidence

ORD record
ord-4e126b73a0cd4caa845167f08b5bc8b2
Source dataset
uspto-grants-2002_04
Patent number
US06372931B1

Reaction notes

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