Ethanolamine → N-(2-hydroxyethyl)-4-methylbenzenesulfonamide
Reaction equation
[C:1]1([CH3:11])[CH:6]=[CH:5][C:4]([S:7](Cl)(=[O:9])=[O:8])=[CH:3][CH:2]=1.[CH2:12]([CH2:14][NH2:15])[OH:13]>>[OH:13][CH2:12][CH2:14][NH:15][S:7]([C:4]1[CH:5]=[CH:6][C:1]([CH3:11])=[CH:2][CH:3]=1)(=[O:9])=[O:8]Participants
3
Procedure
The preparation is carried out as in Example 1(a) but this time 381.3 g of p-toluenesulphonyl chloride (2 mol) and 128.3 g of ethanolamine (2.1 mol) are used for the reaction. The amount obtained is 400.8 g, i.e. a yield of 94.8%.
Workup
- customThe amount obtained
Sources & evidence
- ORD record
- ord-44ea4a17a97346f8ac89b845c9574f44
- Source dataset
- uspto-grants-2002_05
- Patent number
- US06384115B1
Reaction notes
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