Ammonia → HCID 131727910, compound
Reaction equation
C(F)(OC(F)(F)C(F)(F)C(F)(F)F)=C(F)F.[C:17]([O:27][CH:28]([C:30]([O:32]C)=[O:31])[F:29])([C:20]([C:23]([F:26])([F:25])[F:24])([F:22])[F:21])([F:19])[F:18].[NH3:34]>>[C:17]([O:27][CH:28]([C:30]([O-:32])=[O:31])[F:29])([C:20]([C:23]([F:24])([F:25])[F:26])([F:22])[F:21])([F:19])[F:18].[NH4+:34]Participants
4
Procedure
The calculated yield was 59% based on total PPVE used; 70% based on converted PPVE. The ester is converted to the ammonium salt by reaction with aqueous ammonia. Methanol is removed by fractionated distillation. The resulting aqueous solution is used as an emulsifier in the polymerization of fluorinated olefins.
Workup
- customMethanol is removed by fractionated distillation
- customThe resulting aqueous solution is used as an emulsifier in the polymerization of fluorinated olefins
Sources & evidence
- ORD record
- ord-a99cdb66714644ba8381f1cfe23b712b
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08119750B2
Reaction notes
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