Tetrapropylammonium hydroxide → HCID 21079926, compound

HRID 1375302Notes

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-].[CH2:19]([N+:22]([CH2:29][CH2:30][CH3:31])([CH2:26][CH2:27][CH3:28])[CH2:23][CH2:24][CH3:25])[CH2:20][CH3:21]>>[CH2:26]([N+:22]([CH2:19][CH2:20][CH3:21])([CH2:23][CH2:24][CH3:25])[CH2:29][CH2:30][CH3:31])[CH2:27][CH3:28].[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 20586Tetrapropylammonium hydroxide2×

HCID 67815Perfluorobutanesulfonic acid

Product 1

HCID 21079926HCID 21079926, compound

Procedure

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

Sources & evidence

ORD record: ord-ca9084a894a94d888452ff1eda2d21f2
Source dataset: uspto-grants-2007_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07169333B2

Reaction notes

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