Sodium Hydroxide → 1-Bromo-4-methoxy-2,5-dimethylbenzene
Reaction equation
[Br:1]Br.[CH3:3][C:4]1[CH:9]=[CH:8][C:7]([CH3:10])=[CH:6][C:5]=1[O:11][CH3:12].[O-]S([O-])=O.[Na+].[Na+].[OH-].[Na+]>[Fe].O>[Br:1][C:8]1[C:7]([CH3:10])=[CH:6][C:5]([O:11][CH3:12])=[C:4]([CH3:3])[CH:9]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
Bromine (291.5 g, 1835 mmol) was added dropwise with stirring to an initially introduced mixture of 2,5-dimethylanisole (250 g, 1835 mmol) and Fe powder (3.25 g). The commencement of the reaction was evident from gas evolution. The remainder of the bromine was subsequently added dropwise over the course of 30-40 minutes at room temperature with water-bath cooling. The reaction mixture was stirred for about a further 4 hours. The Fe powder was subsequently separated off, a little chloroform was added to the solution, and the solution was washed by shaking with water, resulting in the solution becoming paler. After the solution had been shaken with 50 ml of saturated aqueous Na2SO3 solution, it had become completely colorless. The solution was shaken again with dilute aqueous NaOH and twice with H2O and dried, and the solvent was stripped off. The crude product was subjected to fractional distillation under reduced pressure.
Workup
- temperaturecooling
- customThe Fe powder was subsequently separated off
- additiona little chloroform was added to the solution
- washthe solution was washed
- stirringby shaking with water
- customresulting in the solution
- customdried
- distillationThe crude product was subjected to fractional distillation under reduced pressure
Sources & evidence
- ORD record
- ord-323c195262c74069b9b23f36350f7345
- Source dataset
- uspto-grants-2003_10
- Patent number
- US06638646B2
Reaction notes
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