Sulfuric Acid → 2-Bromo-4-iodo-1-methylbenzene
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[CH3:9])N.S(=O)(=O)(O)O.N([O-])=O.[Na+].[I-:19].[K+]>O>[Br:1][C:2]1[CH:3]=[C:4]([I:19])[CH:6]=[CH:7][C:8]=1[CH3:9]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
To a vigorously stirred mixture of 3-bromo-4-methylaniline (40 g, 215 mmol), sulfuric acid (360 mL) and H2O (900 mL) at 0° C. was added dropwise a NaNO2 solution (16.6 g, 240 mmol in 80 mL of H2O). The mixture was stirred at 0° C. for 1 hour and a solution of potassium iodide (64 g, 387 mmol in 160 mL of H2O) was added. The reaction was stirred for 8 hours at r.t. The aqueous layer was extracted with Et2O and the combined organic layers were washed with a 10% aqueous solution of Na2S2O3, dried over Na2SO4 and concentrated. The residue was filtered through a silica gel pad eluted with 10% EtOAc/hexane and concentrated to give 60 g of the title compound as a reddish syrup used as such.
Workup
- stirringThe reaction was stirred for 8 hours at r.t
- extractionThe aqueous layer was extracted with Et2O
- washthe combined organic layers were washed with a 10% aqueous solution of Na2S2O3
- dry with materialdried over Na2SO4
- concentrationconcentrated
- filtrationThe residue was filtered through a silica gel pad
- washeluted with 10% EtOAc/hexane
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-13776f78ed434af0ba6159c5383045ee
- Source dataset
- uspto-grants-2006_12
- Patent number
- US07144913B2
Reaction notes
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