Hydrochloric Acid → Dimethylsilanediyl bis(trifluoromethanesulfonate)
Reaction equation
Cl[Si:2](Cl)([CH3:4])[CH3:3].[F:6][C:7]([F:13])([F:12])[S:8]([OH:11])(=[O:10])=[O:9].Cl>>[F:6][C:7]([F:13])([F:12])[S:8]([O:11][Si:2]([O:11][S:8]([C:7]([F:13])([F:12])[F:6])(=[O:10])=[O:9])([CH3:4])[CH3:3])(=[O:10])=[O:9]Participants
4
Procedure
An oven-dried 100 mL-RB flask is charged with dichlorodimethylsilane (6.45 g, 0.05 mol). Then trifluoromethanesulfonic acid (15 g, 0.10 mol) is added dropwise. The mixture is heated at 60° C. until no HCl evolves. The residue is distilled to yield 10.7 g (60%) of the product as a clear liquid. 1H NMR (500 MHz, CDCl3, in ppm) δ 0.88 (s, 6H).
Workup
- distillationThe residue is distilled
Sources & evidence
- ORD record
- ord-a6d7098f37ab4a0a827bc4f1759d585c
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08247341B2
Reaction notes
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