Ammonia → HCID 131730347, compound
Reaction equation
[C:1]([C:5]([C:8]([O:11][C:12]([C:15]([C:18]([C:21]([OH:23])=[O:22])([F:20])[F:19])(F)[F:16])([F:14])[F:13])(F)[F:9])([F:7])[F:6])([F:4])([F:3])[F:2].C(C(C(OC(C(C(C(O)=O)(F)F)F)(F)F)F)(F)F)(F)(F)F.[NH3:45].C(C(C(OC(C(C(C([O-])=O)(F)F)(F)F)(F)F)(F)F)(F)F)(F)(F)F.[NH4+]>>[C:1]([C:5]([CH:8]([O:11][C:12]([CH:15]([C:18]([C:21]([O-:23])=[O:22])([F:19])[F:20])[F:16])([F:13])[F:14])[F:9])([F:7])[F:6])([F:4])([F:3])[F:2].[NH4+:45]Participants
5
Procedure
NMR analysis clarified that the fraction 1 was CF3CF2CF2OCF2CF2CF2COOH and the fraction 2 was CF3CF2CHFOCF2CHFCF2COOH. These were neutralized with ammonia so that CF3CF2CF2OCF2CF2CF2COONH4 and CF3CF2CHFOCF2CHFCF2COONH4 were obtained.
Sources & evidence
- ORD record
- ord-0c14634372dc4d308f2d551925073c74
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08969437B2
Reaction notes
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