Hydrochloric Acid → Perfluoro-3-sulfopropanoic acid
Reaction equation
[S:1]([C:6]([C:9]([C:12]([O:14][K])=[O:13])([F:11])[F:10])([F:8])[F:7])([O:4][K])(=[O:3])=[O:2].Cl>O>[S:1]([C:6]([F:7])([F:8])[C:9]([F:10])([F:11])[C:12]([OH:14])=[O:13])([OH:4])(=[O:3])=[O:2].[S:1]([C:6]([C:9]([C:12]([OH:14])=[O:13])([F:10])[F:11])([F:7])[F:8])([OH:4])(=[O:3])=[O:2].[OH2:2].[OH2:2].[OH2:2].[OH2:2].[OH2:2].[OH2:2].[OH2:2].[OH2:2]Participants
5
Reactant 2
Product 2
Reagents, catalysts & solvents 1
Procedure
Ten grams of KO3SCF2CF2COOK were dissolved in 30 ml warm water and placed in a 50 cm×2.5 cm glass column containing a 20 cm bed of "Amberlite IR-120" ion-exchange resin in the acid (H+) form, which had been previously prepared by treating the column with 6 N hydrochloric acid and rinsing with distilled water. The column was eluted with distilled water. The first 150 ml of eluate was concentrated under reduced pressure to yield the hydrate of 3-sulfoperfluoropropionic acid, HO3SCF2CF2COOH.8H2O.
Workup
- additioncontaining a 20 cm bed of "Amberlite
- custom" ion-exchange resin in the acid (H+) form, which had been previously prepared
- washrinsing with distilled water
- washThe column was eluted with distilled water
- concentrationThe first 150 ml of eluate was concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-b7d15cbee2e143128b935883a9b074a0
- Source dataset
- uspto-grants-1982_06
- Patent number
- US04332954
Reaction notes
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