Chlorodifluoromethane → 1-Bromo-3-(difluoromethoxy)-5-fluorobenzene

HRID 1246655Notes

Reaction equation

HRID 1246655 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[C:6]([F:8])[CH:7]=1.Cl[CH:11]([F:13])[F:12]>CC(O)C.[OH-].[K+]>[Br:1][C:2]1[CH:3]=[C:4]([O:9][CH:11]([F:13])[F:12])[CH:5]=[C:6]([F:8])[CH:7]=1

Participants

5

Procedure

A mixture of 3-bromo-5-fluorophenol. (6.1 g, 31.0 mmol; see step (ii) above) and chlorodifluoromethane (13.0 g, 150.0 mmol) in i-PrOH (100 mL) and 30% KOH (80 mL) was heated in a sealed flask for 18 h at 80–85° C. The reaction mixture was cooled to room temperature and the layers were separated. The organic layer was concentrated in vacuo to afford a colourless oil. The aqueous layer was extracted with Et2O (3×30 mL). The crude oil and the combined organic extracts were washed with 2N NaOH (3×30 mL) and H2O (3×30 mL). The organics were then dried (Na2SO4), filtered through a small silica gel plug, and concentrated in vacuo to afford the sub-title compound (6.1 g, 79%) as a colourless oil that was used without further purification.

Workup

  1. customthe layers were separated
  2. concentrationThe organic layer was concentrated in vacuo
  3. customto afford a colourless oil
  4. extractionThe aqueous layer was extracted with Et2O (3×30 mL)
  5. washThe crude oil and the combined organic extracts were washed with 2N NaOH (3×30 mL) and H2O (3×30 mL)
  6. dry with materialThe organics were then dried (Na2SO4)
  7. filtrationfiltered through a small silica gel plug
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-34d6a2bae6964dd8a02671bea58cd5ba
Source dataset
uspto-grants-2006_10
Patent number
US07129233B2

Reaction notes

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