1-Bromo-3-chloro-5-fluorobenzene → 1-Bromo-3-chloro-5-methoxybenzene

HRID 2215353Notes

Reaction equation

HRID 2215353 reaction equation
[CH3:1][O-:2].[Na+].F[C:5]1[CH:10]=[C:9]([Br:11])[CH:8]=[C:7]([Cl:12])[CH:6]=1>CO>[Br:11][C:9]1[CH:10]=[C:5]([O:2][CH3:1])[CH:6]=[C:7]([Cl:12])[CH:8]=1

Participants

4

Procedure

Sodium methoxide (2.20 ml of a 4.5M solution in methanol, 10.0 mmol) was added dropwise to a stirred solution of 1-fluoro-3-chloro-5-bromobenzene (1.00 g, 4.77 mmol) in methanol (28 ml) at room temperature under nitrogen. The reaction was heated under reflux for 3 days and cooled to room temperature. The mixture was concentrated under reduced pressure and the resulting yellow oil was dissolved in dichloromethane (30 ml). The resulting solution was washed with water (2×20 ml) dried over magnesium sulphate, filtered and concentrated under reduced pressure. The crude product was purified by flash column chromatography on silica gel eluting with cyclohexane to provide the title compound (302 mg) as a colourless oil.

Workup

  1. temperatureThe reaction was heated
  2. temperatureunder reflux for 3 days
  3. concentrationThe mixture was concentrated under reduced pressure
  4. dissolutionthe resulting yellow oil was dissolved in dichloromethane (30 ml)
  5. washThe resulting solution was washed with water (2×20 ml)
  6. dry with materialdried over magnesium sulphate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customThe crude product was purified by flash column chromatography on silica gel eluting with cyclohexane

Sources & evidence

ORD record
ord-e5d03c9a3f2943ae9cfdb95c42f24a78
Source dataset
uspto-grants-2006_09
Patent number
US07109228B2

Reaction notes

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