3-Chlorobenzenesulphonyl chloride → HCID 20066941, compound
Reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]#[N:11].[Cl:12][C:13]1[CH:14]=[C:15]([S:19](Cl)(=[O:21])=[O:20])[CH:16]=[CH:17][CH:18]=1>>[Cl:12][C:13]1[CH:14]=[C:15]([S:19]([NH:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][C:2]#[N:1])(=[O:21])=[O:20])[CH:16]=[CH:17][CH:18]=1Participants
3
Procedure
9-Aminononanenitrile (4.0 g, 0.26 mol) was treated with 3-chlorobenzene sulphonyl chloride (5.5 g, 0.26 mol) by the method described in Example 6(i) to give the title compound (4.4 g, m.p. 42°-3° C.).
Sources & evidence
- ORD record
- ord-088f41eaa7594dbe88fce542dff20877
- Source dataset
- uspto-grants-1991_03
- Patent number
- US04997847
Reaction notes
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