Reaktionsgleichung
[C:1]1([S:7]([NH:10][NH2:11])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:12]1(C)[CH:17]=CC(S(O)(=O)=O)=C[CH:13]=1>CC(C)=O>[CH3:13][C:12](=[N:11][NH:10][S:7]([C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)(=[O:8])=[O:9])[CH3:17]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 20 °C
Versuchsvorschrift
A four neck flask (1 liter) equipped with a thermometer, a reflux condenser and a stirrer was charged with 86 g (0.5 mol) of benzenesulfonohydrazide, 0.95 g (0.005 mol) of p-toluenesulfonic acid and 700 ml of acetone and then heated under reflux for about 5 hours. The reaction liquid was cooled down to 20° C. or lower, and then crystal was filtered off and dried under reduced pressure, whereby white crystal was obtained.
Aufarbeitung
- customA four neck flask (1 liter) equipped with a thermometer, a reflux condenser and a stirrer
- temperatureheated
- temperatureunder reflux for about 5 hours
- customThe reaction liquid
- filtrationlower, and then crystal was filtered off
- customdried under reduced pressure, whereby white crystal
- customwas obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-d9380f4f7013413cba21ca57c694bfbf
- Quelldatensatz
- uspto-grants-2002_04
- Patentnummer
- US06380288B1
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