Potassium Bis(trifluoromethanesulfonyl)imide → Diallyldimethylammonium bis(trifluoromethanesulfonyl)imide

HRID 14351Notes

Reaction equation

HRID 14351 reaction equation
[N-:1]([S:9]([C:12]([F:15])([F:14])[F:13])(=[O:11])=[O:10])[S:2]([C:5]([F:8])([F:7])[F:6])(=[O:4])=[O:3].[K+].[Br-].[CH2:18]([N+:21]([CH2:24][CH:25]=[CH2:26])([CH3:23])[CH3:22])[CH:19]=[CH2:20]>>[N-:1]([S:2]([C:5]([F:8])([F:6])[F:7])(=[O:4])=[O:3])[S:9]([C:12]([F:15])([F:14])[F:13])(=[O:11])=[O:10].[CH2:18]([N+:21]([CH2:24][CH:25]=[CH2:26])([CH3:23])[CH3:22])[CH:19]=[CH2:20]

Participants

3

Reactant 2

HCID 11099217Potassium Bis(trifluoromethanesulfonyl)imide2×HCID 13119730Diallyldimethylammonium bromide

Product 1

HCID 11960527Diallyldimethylammonium bis(trifluoromethanesulfonyl)imide

Procedure

Analogous to Example 1, 1-allyl-3-methylimidazolium bromide (AMIBr) produced by the reaction of allylbromide with 1-methylimidazole was reacted with potassium bis[(trifluoromethyl)sulfonyl]imide (KTFSI) to produce AMI TFSI. Similarly, diallyldimethylammonium bis[(trifluoromethyl)sulfonyl]imide (DAA.TFSI) was synthesized from diallyldimethylammonium bromide (DAABr) and KTFSI.

Workup

  1. customto produce AMI TFSI

Sources & evidence

ORD record
ord-81c86296815b42659ca1ddbe1bd6cc79
Source dataset
uspto-grants-2010_06
Patent number
US07732099B2

Reaction notes

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