4-Fluorophenol → Ethyl difluoro(4-fluorophenoxy)acetate

HRID 907603Notes

Reaction equation

HRID 907603 reaction equation
[H-].[Na+].[F:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1.[CH2:11]([O:13][C:14](=[O:19])[C:15](Br)([F:17])[F:16])[CH3:12]>C(OCC)C>[CH2:11]([O:13][C:14](=[O:19])[C:15]([F:17])([F:16])[O:10][C:7]1[CH:8]=[CH:9][C:4]([F:3])=[CH:5][CH:6]=1)[CH3:12]

Participants

5

Procedure

A suspension of 60% of NaH in oil (3.84 g, 96 mmol) was washed three times with hexanes and the solid was suspended in dry DMF (80 ml). 4-Fluorophenol (8.96 g, 80 mmol) was slowly added over a period of 5 min and the reaction mixture was stirred at rt for about 10 min. The reaction mixture was cooled at 0° C. and 2-bromo-2,2-difluoroacetic acid ethyl ester (16.24 g, 80 mmol) was slowly added. The reaction mixture was heated at 90° C. for 20 h. After allowing the reaction to reach room temperature, ethyl ether (300 ml) was added and the suspension was washed with water and brine. After drying the organic layer over sodium sulfate for 15 min, the solvent was evaporated and the crude was purified by flash chromatography, using a mixture of ethyl acetate/hexanes (1/10) to give 2,2-difluoro-2-(4-fluorophenoxy)acetic acid ethyl ester as an oil (11.0 g, 59%).

Workup

  1. washwas washed three times with hexanes
  2. temperatureThe reaction mixture was cooled at 0° C.
  3. temperatureThe reaction mixture was heated at 90° C. for 20 h
  4. customthe reaction
  5. customto reach room temperature
  6. washthe suspension was washed with water and brine
  7. dry with materialAfter drying the organic layer over sodium sulfate for 15 min
  8. customthe solvent was evaporated
  9. customthe crude was purified by flash chromatography
  10. additiona mixture of ethyl acetate/hexanes (1/10)

Sources & evidence

ORD record
ord-22b73e74ccca480e8dc12fc16cddffce
Source dataset
uspto-grants-2011_09
Patent number
US08013186B2

Reaction notes

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