Hydrochloric Acid → 2-Aminomethyl-4-(1,1-dimethylethyl)-6-methylsulfamoylphenol hydrochloride
Reaktionsgleichung
C([NH:4][CH2:5][C:6]1[C:11]([OH:12])=[C:10]([S:13](=[O:17])(=[O:16])[NH:14][CH3:15])[CH:9]=[C:8]([C:18]([CH3:21])([CH3:20])[CH3:19])[CH:7]=1)(=O)C.[ClH:22]>C(O)C>[ClH:22].[NH2:4][CH2:5][C:6]1[CH:7]=[C:8]([C:18]([CH3:20])([CH3:21])[CH3:19])[CH:9]=[C:10]([S:13](=[O:17])(=[O:16])[NH:14][CH3:15])[C:11]=1[OH:12]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
4.9 g (0.016 mole) of 6-acetamidomethyl-4-(1,1-dimethylethyl)-2-methylsulfamoylphenol in a mixture of 30 ml of ethanol and 10 ml of concentrated hydrochloric acid are heated under reflux for 8 hours. Evaporation and recrystallization from methanol/ether gives white crystals of melting point 238°-240° C.
Aufarbeitung
- temperatureare heated
- temperatureunder reflux for 8 hours
- customEvaporation and recrystallization from methanol/ether
- customgives white crystals of melting point 238°-240° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-da580e455ab5437193e566ed18538d68
- Quelldatensatz
- uspto-grants-1988_08
- Patentnummer
- US04766241
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