Water → 5-Bromo-1,3-dichloro-2-(difluoromethoxy)benzene

HRID 551338Notes

Reaction equation

HRID 551338 reaction equation
[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([OH:9])=[C:4]([Cl:10])[CH:3]=1.C(=O)([O-])[O-].[K+].[K+].Br[C:18]([F:25])([F:24])C(OCC)=O.O>C(#N)C>[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([O:9][CH:18]([F:25])[F:24])=[C:4]([Cl:10])[CH:3]=1

Participants

6

Procedure

To a stirred solution of 4-bromo-2,6-dichlorophenol (2.3 g) in acetonitrile (25 mL) was added potassium carbonate (1.3 g) and ethyl bromodifluoroacetate (3.8 g). The mixture was heated to reflux for 4 hours and then cooled to room temperature. The resulting mixture was poured into water (100 mL) and extracted with ethyl acetate (100 mL×1). The organic layer was washed with water and brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to provide a residue. The residue was purified by column chromatography on silica gel eluted with ethyl acetate-hexane (1:4) to afford the title compound as yellow oil (2.4 g).

Workup

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 4 hours
  3. extractionextracted with ethyl acetate (100 mL×1)
  4. washThe organic layer was washed with water and brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customto provide a residue
  8. customThe residue was purified by column chromatography on silica gel
  9. washeluted with ethyl acetate-hexane (1:4)

Sources & evidence

ORD record
ord-e7ee6484490b4f459c8174446d20af6c
Source dataset
uspto-grants-2011_05
Patent number
US07947715B2

Reaction notes

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