Methanesulfonamide → HCID 13013731, compound
Reaction equation
[Cl:1][C:2]1[CH:20]=[C:19]([C:21]([F:24])([F:23])[F:22])[CH:18]=[C:17]([F:25])[C:3]=1[O:4][C:5]1[CH:6]=[CH:7][C:8]([N+:14]([O-:16])=[O:15])=[C:9]([CH:13]=1)[C:10](Cl)=[O:11].[CH3:26][S:27]([NH2:30])(=[O:29])=[O:28]>>[CH3:26][S:27]([NH:30][C:10](=[O:11])[C:9]1[CH:13]=[C:5]([O:4][C:3]2[C:17]([F:25])=[CH:18][C:19]([C:21]([F:24])([F:23])[F:22])=[CH:20][C:2]=2[Cl:1])[CH:6]=[CH:7][C:8]=1[N+:14]([O-:16])=[O:15])(=[O:29])=[O:28]Participants
3
Procedure
Reaction of 5-(2-chloro-6-fluoro-4-trifluoromethylphenoxy)-2-nitro benzoyl chloride with methanesulphonamide to give the required compound, i.e. N-methanesulphonyl-5-(2-chloro-6-fluoro-4-trifluoromethylphenoxy)-2-nitro-benzamide.
Sources & evidence
- ORD record
- ord-708c54847643499cbfe7f11606b69bad
- Source dataset
- uspto-grants-1983_05
- Patent number
- US04384135
Reaction notes
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