Nitrogen → HCID 131735795, compound
Reaction equation
N#N.[C:3]1([PH:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[N-:16]([S:24]([C:27]([F:30])([F:29])[F:28])(=[O:26])=[O:25])[S:17]([C:20]([F:23])([F:22])[F:21])(=[O:19])=[O:18]>CO>[F:30][C:27]([F:28])([F:29])[S:24]([N-:16][S:17]([C:20]([F:21])([F:22])[F:23])(=[O:18])=[O:19])(=[O:25])=[O:26].[C:10]1([PH2+:9][C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 10 °C
Procedure
In a reactor wherein air was replaced by N2, 400.0 g (2.2 mol) of diphenyl phosphine and 400 mL of methanol were added and cooled to 10° C. by a ice-bath. 604.3 g (2.2 mol) of trifluoromethanesulfonimide was then added dropwise under strong stirring. After one hour of reaction, the reaction temperature was increased to about 60° C., and the unreacted materials as well as the solvents were removed by distillation under vacuum to obtain diphenyl phosphonium bis(trifluoromethanesulfonyl)amide.
Workup
- additionwere added
- customAfter one hour of reaction
- temperaturethe reaction temperature was increased to about 60° C.
- customthe unreacted materials as well as the solvents were removed by distillation under vacuum
Sources & evidence
- ORD record
- ord-becf668e84184648a37136fe4e585a04
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09365596B2
Reaction notes
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