2,3,3,3-Tetrafluoro-2-(trifluoromethyl)propanoyl fluoride → Potassium 2,3,3,3-tetrafluoro-2-(trifluoromethyl)propanoate

HRID 3946

Reaction equation

HRID 3946 reaction equation
[F:1][C:2]([C:10]([F:13])([F:12])[F:11])([C:6]([F:9])([F:8])[F:7])[C:3](F)=[O:4].C[Si](C)(C)[O-:16].[K+:19]>CCOCC>[F:1][C:2]([C:10]([F:13])([F:12])[F:11])([C:6]([F:9])([F:8])[F:7])[C:3]([O-:16])=[O:4].[K+:19]

Participants

4

Procedure

Perfluoroisobutyryl fluoride (17.76 g, 82 mmol) was distilled into a 3-neck flask (equipped with a cold finger condenser, mechanical stirrer and a nitrogen inlet) containing a slurry of potassium trimethylsilanolate (10.26 g, 80 mmol) in dry ether (500 mL). The mixture was stirred 3 h at room temperature with the condenser maintained at -40°; then it was cooled to -40° and stirred overnight. The solid was filtered under nitrogen, washed with dry ether, and dried under a stream of nitrogen to afford potassium perfluoroisobutyrate (12.29 g, 61% yield) as a white solid: 19F NMR (D2O) δ -72.2 (d, J=7.5 Hz, CF3, 6F), -171.8 ppm (sp, J=7.5 Hz, CF, 1F). Anal. Calcd. for C4F7KO2 : C, 19.05; F, 52.75. Found: C, 19.12; F, 52.70.

Workup

  1. custom(equipped with a cold finger condenser, mechanical stirrer and a nitrogen inlet)
  2. temperaturemaintained at -40°
  3. temperaturethen it was cooled to -40°
  4. stirringstirred overnight
  5. filtrationThe solid was filtered under nitrogen
  6. washwashed with dry ether
  7. customdried under a stream of nitrogen

Sources & evidence

ORD record
ord-09bf57ad4f744b61bd86e8e655bf212e
Source dataset
uspto-grants-1988_02
Patent number
US04723016

Linked notes

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