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 6N 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-bbf7e3f86e854d9bb560fa8f302256a0
- Source dataset
- uspto-grants-1986_07
- Patent number
- US04600774
Reaction notes
Loading…