Hydrochloric Acid → 2,2,3,3-Tetrafluoro-3-sulfopropanoic acid

HRID 1155780ノート

反応式

HRID 1155780 の反応式
[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]

参加物

5

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-b7d15cbee2e143128b935883a9b074a0
出典データセット
uspto-grants-1982_06
特許番号
US04332954

反応ノート

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