Hydrochloric Acid → Perfluoro-3-sulfopropanoic acid

HRID 1155780Notes

Reaction equation

HRID 1155780 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

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

  1. additioncontaining a 20 cm bed of "Amberlite
  2. custom" ion-exchange resin in the acid (H+) form, which had been previously prepared
  3. washrinsing with distilled water
  4. washThe column was eluted with distilled water
  5. 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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