Boron tribromide → 5-Bromo-2-(1-hydroxy-2-methylpropan-2-yl)phenol
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:12])([CH3:11])[CH2:9][OH:10])=[C:4]([O:13]C)[CH:3]=1.B(Br)(Br)Br>ClCCl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:12])([CH3:11])[CH2:9][OH:10])=[C:4]([OH:13])[CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 2-(4-bromo-2-methoxyphenyl)-2-methylpropan-1-ol (300 mg, 1.16 mmol) in dichloromethane (5 mL) was added dropwise boron tribromide (580 mg, 2.32 mmol) at −78° C. under nitrogen. The reaction mixture was warmed to room temperature and stirred for 30 minutes. The reaction was quenched with water (10 mL) and extracted with dichloromethane (20 mL). The organic layer was washed with aq. sodium bicaronate (20 mL), brine (20 mL), dried over sodium sulfate, filtered and concentrated to give a crude residue, which was purified by flash chromatography to give the title compound (90 mg, 32%) as a white solid.
Workup
- customThe reaction was quenched with water (10 mL)
- extractionextracted with dichloromethane (20 mL)
- washThe organic layer was washed with aq. sodium
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- customto give a crude residue, which
- customwas purified by flash chromatography
Sources & evidence
- ORD record
- ord-a7cbd7f590974038a224646fe6794782
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08889730B2
Reaction notes
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