1-Bromopropane → 4-Cyano-3-propoxybenzenesulfonyl 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]=1[O:13][CH2:14][CH3:15])#[N:2].Br[CH2:17]CC>>[C:1]([C:3]1[CH:8]=[CH:7][C:6]([S:9]([Cl:12])(=[O:11])=[O:10])=[CH:5][C:4]=1[O:13][CH2:14][CH2:15][CH3:17])#[N:2]Participants
3
Procedure
The titled compound was prepared analogously to 4-cyano-3-ethoxy-benzenesulfonyl chloride (Intermediate 127c) by replacing bromoethane with 1-bromopropane.
Sources & evidence
- ORD record
- ord-050ea674e32844198b28eba69d99f79a
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07666878B2
Reaction notes
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