Sulfanium bromide → Sulfonium perfluorobutane sulfonate
Reaction equation
[Br-].[SH3+:2].[F:3][C:4]([F:19])([S:15]([O-:18])(=[O:17])=[O:16])[C:5]([F:14])([F:13])[C:6]([F:12])([F:11])[C:7]([F:10])([F:9])[F:8].[Na+]>[N+](C)([O-])=O>[F:19][C:4]([F:3])([S:15]([O-:18])(=[O:17])=[O:16])[C:5]([F:13])([F:14])[C:6]([F:12])([F:11])[C:7]([F:10])([F:9])[F:8].[SH3+:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The thus obtained monomer precursor is mixed with, for example, phenacyl bromide in acetonitrile or nitromethan at room temperature, to thereby obtain the corresponding sulfonium bromide. With the thus obtained sulfonium bromide, for example, sodium perfluorobutane sulfonate is mixed in nitromethane at room temperature to thereby obtain the targeted product of sulfonium perfluorobutane sulfonate. Moreover, the thus obtained sulfonium perfluorobutanesulfonate can be further purified by recrystallization.
Sources & evidence
- ORD record
- ord-b7f149b3e99a4d5aabb5b4e532189636
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07897321B2
Reaction notes
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