Tetramethylammonium hydroxide → Tetramethylammonium perfluorobutane sulfonate

HRID 1375301

Reaction equation

[F:1][C:2]([F:17])([S:13]([OH:16])(=[O:15])=[O:14])[C:3]([F:12])([F:11])[C:4]([F:10])([F:9])[C:5]([F:8])([F:7])[F:6].[OH-].[CH3:19][N+:20]([CH3:23])([CH3:22])[CH3:21]>>[CH3:19][N+:20]([CH3:23])([CH3:22])[CH3:21].[F:17][C:2]([F:1])([S:13]([O-:16])(=[O:15])=[O:14])[C:3]([F:11])([F:12])[C:4]([F:10])([F:9])[C:5]([F:8])([F:7])[F:6]

Participants

Reactant 2

HCID 60966Tetramethylammonium hydroxide2×

HCID 67815Perfluorobutanesulfonic acid

Product 1

HCID 22620600Tetramethylammonium perfluorobutane sulfonate

Procedure

Perfluorobutanesulfonic acid tetramethylammonium salt is prepared by neutralising perfluorobutanesulfonic acid and tetramethylammonium hydroxide in aqueous solution. Tetramethylammonium hydroxide is obtainable from Aldrich.

Sources & evidence

ORD record: ord-ca1d896ccdff475aacad1417666e002e
Source dataset: uspto-grants-2007_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07169333B2

Linked notes

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