Perfluorooctanesulfonic acid → Silver perfluorooctanesulfonate

HRID 1934291Notes

Reaction equation

HRID 1934291 reaction equation
[F:1][C:2]([F:29])([S:25]([OH:28])(=[O:27])=[O:26])[C:3]([F:24])([F:23])[C:4]([F:22])([F:21])[C:5]([F:20])([F:19])[C:6]([F:18])([F:17])[C:7]([F:16])([F:15])[C:8]([F:14])([F:13])[C:9]([F:12])([F:11])[F:10].C(=O)([O-])[O-].[Ag+2:34]>O>[F:29][C:2]([F:1])([S:25]([O-:28])(=[O:27])=[O:26])[C:3]([F:23])([F:24])[C:4]([F:22])([F:21])[C:5]([F:19])([F:20])[C:6]([F:18])([F:17])[C:7]([F:16])([F:15])[C:8]([F:14])([F:13])[C:9]([F:12])([F:11])[F:10].[Ag+:34]

Participants

4

Procedure

Into a four-necked flask were charged 75 parts of perfluorooctanesulfonic acid and 100 parts of water, and 21.4 parts of silver carbonate was added thereto with stirring. After stirring at room temperature for 3 days, the mixture was filtered and the obtained filter-cake was washed with 10 parts of ion-exchange water, then 20 parts of diethylether and dried to give 60.3 parts of silver perfluorooctanesulfonate.

Workup

  1. additionwas added
  2. stirringAfter stirring at room temperature for 3 days
  3. filtrationthe mixture was filtered
  4. filtrationthe obtained filter-cake
  5. washwas washed with 10 parts of ion-exchange water
  6. dry with material20 parts of diethylether and dried

Sources & evidence

ORD record
ord-47c359f0ed784570aaf73317d365bc12
Source dataset
uspto-grants-2002_05
Patent number
US06383713B1

Reaction notes

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