Hydrogen Bromide → 4-Hydroxyphenylacetone
Reaction equation
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10](=[O:12])[CH3:11])=[CH:5][CH:4]=1.Br>C(O)(=O)C>[OH:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:9][C:10](=[O:12])[CH3:11])=[CH:7][CH:8]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 82 g of 1-(4-methoxyphenyl)-2-propanone, 500 ml of acetic acid and 500 ml of aqueous hydrobromic acid is boiled under reflux for 2 hours and then evaporated in vacuo. The oily residue is extracted four times with 700 ml of hexane/ether (5:2) each time, the extract is evaporated and the residue is chromatographed over silica gel using hexane/ethyl acetate (3:1). 1-(4-Hydroxyphenyl)-2-propanone is thus obtained with a melting point of 40-41°.
Workup
- temperatureunder reflux for 2 hours
- customevaporated in vacuo
- extractionThe oily residue is extracted four times with 700 ml of hexane/ether (5:2) each time
- customthe extract is evaporated
- customthe residue is chromatographed over silica gel
Sources & evidence
- ORD record
- ord-998f1256427149a4bb4a549fd8a1b4a4
- Source dataset
- uspto-grants-2000_12
- Patent number
- US06156923
Reaction notes
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