Reaction equation
[Br-].[CH2:2]([S+:11]1[CH2:15][CH2:14][CH2:13][CH2:12]1)[C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:4].[F:16][C:17]([F:23])([F:22])[S:18]([OH:21])(=[O:20])=[O:19]>>[F:16][C:17]([F:23])([F:22])[S:18]([O-:21])(=[O:20])=[O:19].[CH2:2]([S+:11]1[CH2:15][CH2:14][CH2:13][CH2:12]1)[C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:4]Participants
3
Procedure
Compound (III-2) was synthesized by salt exchange of phenacyltetrahydrothiophenium bromide with trifluoromethanesulfonic acid in the same manner as above.
Sources & evidence
- ORD record
- ord-7fd18d511ffa44e3aae56cd4eb320978
- Source dataset
- uspto-grants-2005_02
- Patent number
- US06858370B2
Linked notes
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