Phenylacetone → (S)-1-Phenyl-2-propanol

HRID 349152Notes

Reaction equation

HRID 349152 reaction equation
[C:1]1([CH2:7][C:8](=[O:10])[CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>O>[C:1]1([CH2:7][C@@H:8]([OH:10])[CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

3

Procedure

Washed phaseolus aureus L (green grams) 50 g. were taken into a conical flask and allowed to soak in deionised water (400 ml) for a period of 24 hr. Phenylacetone (0.500 g; 0.0037 moles) I(d) was added to the soaked phaseolus aureus L (green grams) in the above water, covered and allowed to shake for 24 hr at 15–20° C. Then the green grams were filtered off and washed with deionised water (3×100 ml). The combined filtrate was extracted with chloroform (3×500 ml). The chloroform layer was dried and the crude product obtained (330 mg). Pure 1-phenyl-(2S)-propan-2-ol II(d) was obtained after column chromatography with silica gel using chloroform as eluent.

Workup

  1. washWashed phaseolus aureus L (green grams) 50 g
  2. customwere taken into a conical flask
  3. waitto shake for 24 hr at 15–20° C
  4. filtrationThen the green grams were filtered off
  5. washwashed with deionised water (3×100 ml)
  6. extractionThe combined filtrate was extracted with chloroform (3×500 ml)
  7. dry with materialThe chloroform layer was dried
  8. customthe crude product obtained (330 mg)

Sources & evidence

ORD record
ord-0e45f24e1424433c8d28cc9fcc5f3eef
Source dataset
uspto-grants-2007_02
Patent number
US07179624B2

Reaction notes

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