Benzenesulfonyl chloride → HCID 15329854, compound
Reaction equation
[C:1]1([S:7](Cl)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][OH:17]>>[OH:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][NH:11][S:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)(=[O:9])=[O:8]Participants
3
Procedure
The preparation is carried out as in Example 1(a) from 353 g (2 mol) of benzenesulphonyl chloride and 216.6 g (2.1 mol) of 5-amino-1-pentanol. Yield: 476.8 g, i.e. 98%.
Sources & evidence
- ORD record
- ord-4c30b91ddba446b79a26aedc5aa03f9f
- Source dataset
- uspto-grants-2002_05
- Patent number
- US06384115B1
Reaction notes
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