2-(2-chlorobenzenesulfonyl) acetonitrile → 2-(2-Chlorobenzene-1-sulfonyl)-3,3-di(methanesulfonyl)prop-2-enenitrile
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8]([CH2:11][C:12]#[N:13])(=[O:10])=[O:9].ClC1C=C[C:18]([S:21]([CH2:24]C#N)(=[O:23])=[O:22])=CC=1>>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8]([C:11](=[C:24]([S:8]([CH3:3])(=[O:10])=[O:9])[S:21]([CH3:18])(=[O:23])=[O:22])[C:12]#[N:13])(=[O:10])=[O:9]Participants
3
Procedure
The titled compound was prepared in an analogous fashion to Intermediate 2 except that 2-(2-chlorobenzenesulfonyl) acetonitrile is utilized in place of 2-(4-chlorobenzenesulfonyl) acetonitrile.
Sources & evidence
- ORD record
- ord-fcb8dd93ac3346b6b6701f8b8fc6a3c5
- Source dataset
- uspto-grants-2005_04
- Patent number
- US06875771B2
Reaction notes
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