Reaktionsgleichung
[S:1]1(=O)[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1.[N+:11]([O-])([OH:13])=[O:12].C(OC(=O)C)(=[O:17])C>>[N+:11]([C:7]1[CH:8]=[CH:9][C:4]2[NH:3][C:2](=[O:17])[S:1][C:5]=2[CH:6]=1)([O-:13])=[O:12]Komponenten
4
Reaktionsbedingungen
- Temperatur
- -10 °C
Versuchsvorschrift
0.1 mol of benzothiazolinone is dissolved in 100 ml of acetic anhydride and the solution is cooled to −10° C. 10 ml of nitric acid are then added dropwise, and the reaction is stirred for 2 hours. The resulting precipitate is filtered off and washed with water, and then purified by chromatography (eluant CH2Cl2 then AcOEt) to yield the title product, which is recrystallised from ethanol.
Aufarbeitung
- filtrationThe resulting precipitate is filtered off
- washwashed with water
- custompurified by chromatography (eluant CH2Cl2
Quellen und Nachweise
- ORD-Eintrag
- ord-1fbddb1298af4da6a2867526236a7614
- Quelldatensatz
- uspto-grants-2005_07
- Patentnummer
- US06919362B2
Verknüpfte Notizen
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