Trifluoromethanesulfonic anhydride → HCID 87422849, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[C:11](=[O:12])[C:10]3[CH:13]=[CH:14][CH:15]=[C:16]([OH:17])[C:9]=3[CH2:8][CH2:7][C:6]=2[CH:18]=1.[O:19](S(C(F)(F)F)(=O)=O)[S:20]([C:23]([F:26])([F:25])[F:24])(=O)=[O:21]>N1C=CC=CC=1>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[C:11](=[O:12])[C:10]3[CH:13]=[CH:14][CH:15]=[C:16]([O:17][S:20]([C:23]([F:26])([F:25])[F:24])(=[O:21])=[O:19])[C:9]=3[CH2:8][CH2:7][C:6]=2[CH:18]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
For the preparation of the title compound, 0.517 g (0.0020 mol) of 8-chloro-1-hydroxy-10,11-dihydrodibenzo[a,d]cyclohepten-5-one and 0.846 g (0.0030 mol) of Tf2O in 5 ml of pyridine are reacted by method R. C16H10ClF3O4S (Mr=390.77); GC 11.9 min
Sources & evidence
- ORD record
- ord-246f9384960f43a5969870fcf1028833
- Source dataset
- uspto-grants-2014_01
- Patent number
- US08633312B2
Reaction notes
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