Perfluorobutanesulfonic acid → HCID 131726216, compound

HRID 1375303Notes

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+:25]([CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43])([CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH3:37])[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[CH2:20][CH2:21][CH2:22][CH2:23][CH3:24]>>[CH2:38]([N+:25]([CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])([CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH3:37])[CH2:39][CH2:40][CH2:41][CH2:42][CH3:43].[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 67815Perfluorobutanesulfonic acid

HCID 13998878N,N,N-Trihexylhexan-1-aminium hydroxide2×

Product 1

HCID 131726216HCID 131726216, compound

Procedure

Perfluorobutanesulfonic acid tetrahexylammonium salt is prepared by neutralising perfluorobutanesulfonic acid and tetrahexylammonium hydroxide in aqueous solution. Tetrahexylammonium hydroxide is obtainable from Fluka.

Sources & evidence

ORD record: ord-55d8dbee17904a20bf15bd21c4383e07
Source dataset: uspto-grants-2007_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07169333B2

Reaction notes

Loading…