Reaktionsgleichung
[S:1](=[O:5])(=O)([OH:3])[OH:2].Cl.[C:7]([C:10]1[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][CH:11]=1)(=[NH:9])[NH2:8]>>[C:7]([C:10]1[CH:11]=[CH:12][C:13]([OH:16])=[C:14]([S:1]([OH:3])(=[O:5])=[O:2])[CH:15]=1)(=[NH:8])[NH2:9]Komponenten
3
Versuchsvorschrift
To 15 ml of 60% fuming sulfuric acid, while being cooled in ice, was added slowly 10.0 g of 4-amidinophenol hydrochloride. After the addition, the mixture was stirred at room temperature for 4 hours, then poured slowly into 200 ml of ice water, and stirred for a while. The colorless solid which was precipitated was collected by filtration, washed with water, then with acetone, and dried to obtain 10.2 g of 5-amidino-2-hydroxybenzenesulfonic acid.
Aufarbeitung
- additionAfter the addition
- stirringstirred for a while
- customThe colorless solid which was precipitated
- filtrationwas collected by filtration
- washwashed with water
- dry with materialwith acetone, and dried
Quellen und Nachweise
- ORD-Eintrag
- ord-998a82fd747b49988d27537fe1ff269a
- Quelldatensatz
- uspto-grants-1986_02
- Patentnummer
- US04570006
Verknüpfte Notizen
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