Acetic Anhydride → N-[4-(trifluoromethylsulfonyl)phenyl]acetamide
Reaction equation
[F:1][C:2]([F:14])([F:13])[S:3]([C:6]1[CH:11]=[CH:10][C:9]([NH2:12])=[CH:8][CH:7]=1)(=[O:5])=[O:4].[CH3:15][C:16](OC(C)=O)=[O:17]>CC(O)=O>[F:14][C:2]([F:13])([F:1])[S:3]([C:6]1[CH:7]=[CH:8][C:9]([NH:12][C:16](=[O:17])[CH3:15])=[CH:10][CH:11]=1)(=[O:4])=[O:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Reflux 4-trifluoromethylsulfonyl-phenylamine (5 g) and Ac2O (2.2 mL) for 1.5 hours in HOAc (20 mL). Evaporate the solvent in vacuo, then crystallize the residue in EtOAc/EtOH to obtain N-(4-trifluoromethylsulfonyl-phenyl)-acetamide.
Workup
- customEvaporate the solvent in vacuo
- customcrystallize the residue in EtOAc/EtOH
Sources & evidence
- ORD record
- ord-125f61f384cb41d79571437b1b5a78a5
- Source dataset
- uspto-grants-2003_05
- Patent number
- US06566367B2
Reaction notes
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