2-Methyl-4-nitrobenzonitrile → 4-Cyano-3-methylbenzenesulfonyl chloride
Reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([S:9]([Cl:12])(=[O:11])=[O:10])=[CH:5][C:4]=1OCC)#[N:2].[CH3:16]C1C=C([N+]([O-])=O)C=CC=1C#N>>[C:1]([C:3]1[CH:8]=[CH:7][C:6]([S:9]([Cl:12])(=[O:10])=[O:11])=[CH:5][C:4]=1[CH3:16])#[N:2]Participants
3
Procedure
The titled compound was prepared analogously to 4-cyano-3-ethoxy-benzenesulfonyl chloride (Intermediate 127c) by replacing 2-ethoxy-4-nitro-benzonitrile with 2-methyl-4-nitro-benzonitrile.
Sources & evidence
- ORD record
- ord-28cf79bc53114fe5b25453b48ef0d266
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07666878B2
Reaction notes
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