Benzenesulfonyl chloride → N-(3-Hydroxypropyl)benzenesulfonamide
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][OH:15]>>[OH: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 of benzenesulphonyl chloride (2 mol) and 157.7 g of 3-amino-1-propanol (2.1 mol).
Sources & evidence
- ORD record
- ord-862c5e29c4234e8caa16556f84f02df9
- Source dataset
- uspto-grants-2003_09
- Patent number
- US06624218B2
Reaction notes
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