Butyl bromide → HCID 86620151, compound
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][CH2:18]CC>>[CH2:14]([O:13][C:4]1[CH:5]=[C:6]([S:9]([Cl:12])(=[O:11])=[O:10])[CH:7]=[CH:8][C:3]=1[C:1]#[N:2])[CH2:15][CH2:17][CH3:18]Participants
3
Procedure
The titled compound was prepared analogously to 4-cyano-3-ethoxy-benzenesulfonyl chloride (Intermediate 127c) by replacing bromoethane with 1-bromobutane.
Sources & evidence
- ORD record
- ord-583617f060094ca0adb8e53706a37201
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07666878B2
Reaction notes
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