Phenylacetone → (S)-1-Phenyl-2-propanol
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]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
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
- washWashed phaseolus aureus L (green grams) 50 g
- customwere taken into a conical flask
- waitto shake for 24 hr at 15–20° C
- filtrationThen the green grams were filtered off
- washwashed with deionised water (3×100 ml)
- extractionThe combined filtrate was extracted with chloroform (3×500 ml)
- dry with materialThe chloroform layer was dried
- 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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