4-Chlorobenzoic Acid → 2-Chloro-5-(4-methoxy-benzoyl)-benzenesulfonyl chloride
Reaction equation
F[C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:17])[C:9]2[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][CH:10]=2)=[CH:4][C:3]=1[S:18]([Cl:21])(=[O:20])=[O:19].[Cl:22]C1C=CC(C(O)=O)=CC=1>>[Cl:22][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:17])[C:9]2[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[CH:11][CH:10]=2)=[CH:4][C:3]=1[S:18]([Cl:21])(=[O:20])=[O:19]Participants
3
Procedure
The title compound is prepared as described above for 2-fluoro-5-(4-methoxy-benzoyl)-benzenesulfonyl chloride, starting with 4-chloro-benzoic acid.
Sources & evidence
- ORD record
- ord-3a65a9774a324b41970f0851bb584428
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08975439B2
Reaction notes
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