Trifluoromethanesulfonic anhydride → HCID 86618071, compound
Reaction equation
FC(F)(F)S([O:6][S:7]([C:10]([F:13])([F:12])[F:11])(=[O:9])=[O:8])(=O)=O.[C:16]([C:18]1[CH:19]=[C:20]([C:25]2[S:29][C:28]([C:30]([O:32][CH3:33])=[O:31])=[CH:27][CH:26]=2)[CH:21]=[CH:22][C:23]=1O)#[N:17]>N1C=CC=CC=1>[C:16]([C:18]1[CH:19]=[C:20]([C:25]2[S:29][C:28]([C:30]([O:32][CH3:33])=[O:31])=[CH:27][CH:26]=2)[CH:21]=[CH:22][C:23]=1[O:6][S:7]([C:10]([F:11])([F:12])[F:13])(=[O:8])=[O:9])#[N:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Trifluoromethanesulfonic anhydride was added to a pyridine solution of methyl 5-(3-cyano-4-hydroxyphenyl)thiophene-2-carboxylate and the whole was stirred at room temperature to obtain methyl 5-(3-cyano-4-{[(trifluoromethyl)sulfonyl]oxy}phenyl)thiophene-2-carboxylate. F: 392.
Sources & evidence
- ORD record
- ord-1d7d08277cac40719cee78cfe86464d2
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07612108B2
Reaction notes
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