Hydrochloric Acid → 3-Bromo-4-methoxyaniline

HRID 434155Notes

Reaction equation

HRID 434155 reaction equation
[Br:1][C:2]1[CH:7]=[C:6]([N+:8]([O-])=O)[CH:5]=[CH:4][C:3]=1[O:11][CH3:12].C(O)C.Cl.[OH-].[Na+]>[Fe].O>[NH2:8][C:6]1[CH:5]=[CH:4][C:3]([O:11][CH3:12])=[C:2]([Br:1])[CH:7]=1

Participants

7

Procedure

To a mixture of 2-bromo-4-nitroanisole (5.0 g, 21.5 mmol, Lancaster), ethanol (25 mL) and water (25 mL), was added powdered iron (4.8 g, 86 mmol) and 12 N HCl (0.5 mL). The solution was heated at reflux for 20 minutes. 1N NaOH (10 mL) was added and the reaction mixture was filtered through a pad of celite while still hot, and then rinsed with ethanol (2×50 mL). The ethanol was removed under reduced pressure and the residue extracted with dichloromethane (2×100 mL). The organic extracts were dried (Na2SO4) and concentrated. The crude product was purified by flash chromatography on silica gel (75 g) eluting with dichloromethane, to give 4-amino-2-bromoanisole as a light tan solid.

Workup

  1. temperatureThe solution was heated
  2. temperatureat reflux for 20 minutes
  3. filtrationthe reaction mixture was filtered through a pad of celite while still hot, and
  4. washthen rinsed with ethanol (2×50 mL)
  5. customThe ethanol was removed under reduced pressure
  6. extractionthe residue extracted with dichloromethane (2×100 mL)
  7. dry with materialThe organic extracts were dried (Na2SO4)
  8. concentrationconcentrated
  9. customThe crude product was purified by flash chromatography on silica gel (75 g)
  10. washeluting with dichloromethane

Sources & evidence

ORD record
ord-c10f3909aae84fefaf7e39817cc6ab0e
Source dataset
uspto-grants-2003_12
Patent number
US06670376B1

Reaction notes

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