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Bromine → 1-Bromo-4-methoxy-2,5-dimethylbenzene

HRID 430876
Notes
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Reaction equation

HRID 430876 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]>[Fe]>[Br:1][C:8]1[C:7]([CH3:10])=[CH:6][C:5]([O:11][CH3:12])=[C:4]([CH3:3])[CH:9]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24408Bromine2×HCID 743502,5-Dimethylanisole

Product 1

HCID 27525981-Bromo-4-methoxy-2,5-dimethylbenzene

Reagents, catalysts & solvents 1

HCID 23925IronCatalyst

Procedure

Bromine (291.5 g, 1835 mmol) was added dropwise to a mixture of 2,5-dimethylanisole (250 g, 1835 mmol) and Fe powder (3.25 g) while stirring. The commencement of the reaction could be observed by means of the evolution of gas. The remaining bromine was then added dropwise over a period of 30-40 minutes at room temperature while cooling on a water bath. The reaction mixture was stirred further for about 4 hours. The solution was subsequently separated from the Fe powder, a little chloroform was added and the mixture was shaken with water, leading to the solution becoming lighter in color. After shaking with 50 ml of saturated aqueous Na2SO3 solution, the solution had become completely decolorized. It was shaken once more with dilute aqueous NaOH and twice with H2O and, after drying, the solvent was taken off. The crude product was fractionally distilled under reduced pressure.

Workup

  1. customThe commencement of the reaction
  2. temperaturewhile cooling on a water bath
  3. stirringThe reaction mixture was stirred further for about 4 hours
  4. customThe solution was subsequently separated from the Fe powder
  5. additiona little chloroform was added
  6. stirringthe mixture was shaken with water
  7. stirringAfter shaking with 50 ml of saturated aqueous Na2SO3 solution
  8. stirringIt was shaken once more with dilute aqueous NaOH and twice with H2O
  9. customafter drying
  10. distillationThe crude product was fractionally distilled under reduced pressure

Sources & evidence

ORD record
ord-3a6e8c6291cd4d35bea2908dd1a75591
Source dataset
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06323373B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes