4-Nitrobenzenesulfonyl chloride → N-benzyl-4-nitrobenzenesulfonamide
Reaction equation
NCc1ccccc1.O=[N+]([O-])c1ccc(S(=O)(=O)Cl)cc1>CC(C)=O.O.O=C([O-])O.OCCOCCOCCOCCOCCO.[Na+]>O=[N+]([O-])c1ccc(S(=O)(=O)NCc2ccccc2)cc1Participants
7
Conditions
- Temperature
- 25 °C
Workup
- additionNo procedure recorded
- extractionKeep organic
- washNo procedure recorded
- washNo procedure recorded
- dry with materialNo procedure recorded
- concentrationNo procedure recorded
Sources & evidence
- ORD record
- ord-460799004ab944a2a387bfaf2dda9bb0
- Source dataset
- 39 compound library from "Building a Sulfonamide Library by Eco-Friendly Flow Synthesis"
- Original link
- View source
Reaction notes
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