Trifluoromethanesulfonic anhydride → HCID 22506078, compound
Reaction equation
[CH2:1]([Si:9]([CH3:14])([CH3:13])N(C)C)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[F:15][C:16]([F:29])([F:28])[S:17]([O:20]S(C(F)(F)F)(=O)=O)(=[O:19])=[O:18]>>[F:15][C:16]([F:29])([F:28])[S:17]([O:20][Si:9]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])([CH3:14])[CH3:13])(=[O:19])=[O:18]Participants
3
Procedure
Additionally, for example when mixing octyldimethyl(dimethylamino)silane as the silicon compound B and trifluoromethanesulfonic anhydride as the acid B, the trifluoromethanesulfonic anhydride is rapidly reacted to form octyldimethylsilyl trifluoromethanesulfonate as the acid A.
Sources & evidence
- ORD record
- ord-f3f84c4464534b1091a329016049614f
- Source dataset
- uspto-grants-2016_01
- Patent number
- US09228120B2
Reaction notes
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