Hydrochloric Acid → Sodium 2-(2-hydroxyethyl)amino-5-nitrobenzenesulphinate
Reaction equation
Cl[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[S:11]([O-:13])=[O:12].[Na+:14].[CH2:15]([CH2:17][NH2:18])[OH:16].Cl>O>[OH:16][CH2:15][CH2:17][NH:18][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[S:11]([O-:13])=[O:12].[Na+:14]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
122 g of sodium 2-chloro-5-nitrobenzenesulphinate are kneaded together with 150 g of ethanolamine, and the mixture is gradually heated to 100° C. After 30 minutes at 100° C. 500 ml of water are added, the reaction solution is neutralised with hydrochloric acid, and the sodium 2-(2-hydroxyethyl)amino-5-nitrobenzenesulphinate is isolated as above, by salting out.
Sources & evidence
- ORD record
- ord-2abea71c554d4ade8c590de5913dfe09
- Source dataset
- uspto-grants-1986_03
- Patent number
- US04577015
Reaction notes
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