Sodium Hydroxide → 4-Bromo-2-methoxyphenol
Reaction equation
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([Br:9])=[CH:5][C:4]=1[O:10][C:11](=O)OC1C=C(Br)C=CC=1OC.[OH-].[Na+]>CO>[Br:9][C:6]1[CH:5]=[C:4]([O:10][CH3:11])[C:3]([OH:2])=[CH:8][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A suspension of (20.7 g, 47.9 mmol, 1.0 eq) bis(2-methoxy-5-bromophenyl)carbonate in 250 ml methanol and 60 ml (120 mmol, 2.5 eq) of 2N NaOH was refluxed for 2 hours. The reaction mixture was cooled to room temperature, concentrated to a volume of ca 100 ml, and poured 1 L of H2O. The pH was adjusted to 2 using 1N HCl. The acidic mixture was transferred to a separatory funnel, and extracted three times with ether. The ether extracts were combined and washed once with H2 O, once with brine, and then dried over anhydrous sodium sulfate. Filtration, concentration and drying afforded 19.0 g of a white solid, which was recrystallized from petroleum ether to yield 17.63 g, 91% yield, of white prisms.
Workup
- temperaturewas refluxed for 2 hours
- concentrationconcentrated to a volume of ca 100 ml
- additionpoured 1 L of H2O
- customThe acidic mixture was transferred to a separatory funnel
- extractionextracted three times with ether
- washwashed once with H2 O, once with brine
- dry with materialdried over anhydrous sodium sulfate
- filtrationFiltration, concentration
- customdrying
Sources & evidence
- ORD record
- ord-e4084e86093146c485d0819c045a61dd
- Source dataset
- uspto-grants-1998_09
- Patent number
- US05814651
Reaction notes
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