Sulfanium bromide → Sulfonium perfluorobutane sulfonate

HRID 597756Notes

Reaction equation

HRID 597756 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

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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