Potassium Bicarbonate → HCID 178526055, compound
Reaction equation
[C:1](=[O:4])([O-])[OH:2].[K+:5].[C:6]([O:22][C:23]([C:26]([C:29]([O:32][C:33](C(F)=O)([C:35]([F:38])([F:37])[F:36])[F:34])([F:31])[F:30])([F:28])[F:27])([F:25])[F:24])([C:15]([S:18]([F:21])(=[O:20])=[O:19])([F:17])[F:16])([C:8]([S:11]([F:14])(=[O:13])=[O:12])([F:10])[F:9])[F:7]>C(COC)OC>[C:6]([O:22][C:23]([C:26]([C:29]([O:32][C:33]([C:1]([O:2][K:5])=[O:4])([C:35]([F:38])([F:37])[F:36])[F:34])([F:31])[F:30])([F:28])[F:27])([F:25])[F:24])([C:15]([S:18]([F:21])(=[O:20])=[O:19])([F:17])[F:16])([C:8]([S:11]([F:14])(=[O:13])=[O:12])([F:10])[F:9])[F:7]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Potassium hydrogen carbonate (6.03 g) was charged into a flask together with monoglyme (59 mL), and (FSO2CF2)2CFOCF2CF2CF2OCF(CF3)COF (35.6 g) obtained in Example 3 was added dropwise thereto with stirring under cooling with ice. Vacuum drying was carried out for 30 minutes and then vacuum drying was further carried out at 120° C. for 48 hours to obtain (FSO2CF2)2CFOCF2CF2CF2OCF(CF3)COOK (21.1 g). The obtained (FSO2CF2)2CFOCF2CF2CF2OCF(CF3)COOK was heated at 200° C. under 400 Pa (absolute pressure), and generated gas was collected in a trap cooled with liquid nitrogen to obtain a liquid (8.35 g). The liquid was analyzed by NMR and GC and as a result, formation of the title compound (NMR yield: 25%, GC purity: 87%) was confirmed. Further, as another component, formation of (FSO2CF2)2CFOCF2CF2CF2OCFHCF3 was confirmed.
Workup
- additionwas added dropwise
- temperatureunder cooling with ice
- customVacuum drying
- customvacuum drying
- waitwas further carried out at 120° C. for 48 hours
Sources & evidence
- ORD record
- ord-4c74e5cc0e884c47915b9ddeb435618e
- Source dataset
- uspto-grants-2007_11
- Patent number
- US07297815B2
Reaction notes
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