Cesium carbonate → 3-(Difluoromethoxy)bromobenzene

HRID 2098909Notes

Reaction equation

HRID 2098909 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[CH:6][CH:7]=1.Cl[C:10]([F:15])([F:14])C([O-])=O.[Na+].C(=O)([O-])[O-].[Cs+].[Cs+]>CN(C=O)C.CCOC(C)=O>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([O:8][CH:10]([F:15])[F:14])[CH:3]=1

Participants

6

Conditions

Temperature
100 °C

Procedure

To a solution of 3-bromophenol (available from Sigma Aldrich) (1.28 g, 7.39 mmol) in DMF (12.0 mL) was added sodium 2-chloro-2,2-difluoroacetate (available from Sigma Aldrich) (2.82 g, 18.49 mmol) and cesium carbonate (4.82 g, 14.79 mmol). The reaction mixture was heated at 100° C. Gas was released from the reaction so care should be taken. After 2 hours, the reaction was cooled to room temperature then diluted with EtOAc, washed with water and then brine and re-extracted three times with EtOAc. The combined organic layers were dried over magnesium sulfate and then filtered, concentrated, and purified with silica gel chromatography (0-5% EtOAc in hexanes) to yield T7.1 as an oil that was used without further purification (yield 61%).

Workup

  1. customGas was released from the reaction so care
  2. temperaturethe reaction was cooled to room temperature
  3. washwashed with water
  4. extractionbrine and re-extracted three times with EtOAc
  5. dry with materialThe combined organic layers were dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. custompurified with silica gel chromatography (0-5% EtOAc in hexanes)
  9. customto yield T7.1 as an oil that
  10. customwas used without further purification (yield 61%)

Sources & evidence

ORD record
ord-242983844eba45088f190dcb6bddff26
Source dataset
uspto-grants-2013_05
Patent number
US08450522B2

Reaction notes

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