Caprolactam → HCID 86610174, compound
Reaction equation
[C:1]1(=[O:8])[NH:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[F:9][B-:10]([F:13])([F:12])[F:11].[H+]>>[F:9][B-:10]([F:13])([F:12])[F:11].[C:1]1(=[O:8])[NH:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
3
Procedure
The procedure is the same as in example 2 except that the amount of ε-caprolactam and tetrafluoroboric acid added is increased to 1 mol respectively. Desired product of caprolactam tetrafluoroborate was obtained with a yield of 96.3%. No melting point was observed. The density, the viscosity, the ionic conductivity, the glass transition temperature, and the Hammett acidic scale H0 are the same as those of in example 2.
Workup
- additionadded
- temperatureis increased to 1 mol respectively
Sources & evidence
- ORD record
- ord-88a6c0e695924b01a09452025f4ed1df
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07220869B2
Reaction notes
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