Lithium hydroxide, monohydrate → HCID 178506958, compound
Reaction equation
[S:1]([C:7]([C:10]([C:13]([C:16]([S:19](F)(=O)=[O:20])([F:18])[F:17])([F:15])[F:14])([F:12])[F:11])([F:9])[F:8])([F:6])([F:5])([F:4])([F:3])[F:2].[OH:23][Li:24].[OH2:25]>CO>[S:1]([C:7]([C:10]([C:13]([C:16]([S:19]([O:23][Li:24])(=[O:20])=[O:25])([F:18])[F:17])([F:15])[F:14])([F:12])[F:11])([F:9])[F:8])([F:5])([F:4])([F:3])([F:2])[F:6]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A 10-gram mixture of F5S(CF2)4SO2F (47.5 wt %) and cyclo-SF4C4F7SO2F (52 wt %) was charged to a flask containing LiOH.H2O (2.3 g) slurried in 30 g methanol. The reaction mixture was refluxed 18 hrs and then cooled to room temperature. The LiF was then filtered away. The cake was washed with an additional 30 mL methanol. The filtrate was placed in a dish and placed in an oven at 80° C. overnight. A total of 5.5 g of lithium salt, an off-white solid, was removed from the dish. IR analysis of the solid was consistant for the desired lithium salt: F5S(CF2)4SO3Li.
Workup
- temperatureThe reaction mixture was refluxed 18 hrs
- filtrationThe LiF was then filtered away
- washThe cake was washed with an additional 30 mL methanol
- customA total of 5.5 g of lithium salt, an off-white solid, was removed from the dish
Sources & evidence
- ORD record
- ord-9c9de7dbd8e046f38f24f80513e2b8f1
- Source dataset
- uspto-grants-1994_02
- Patent number
- US05286352
Reaction notes
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