Reaktionsgleichung
Cl.C(O[C:5](=[NH:16])[CH2:6][S:7]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)(=[O:9])=[O:8])C.[OH-].[Na+].[CH3:19][C:20]1[CH:21]=[C:22]([C:26]([NH:28][NH2:29])=[O:27])[O:23][C:24]=1[CH3:25]>C(Cl)(Cl)Cl>[NH2:16][C:5](=[N:29][NH:28][C:26]([C:22]1[O:23][C:24]([CH3:25])=[C:20]([CH3:19])[CH:21]=1)=[O:27])[CH2:6][S:7]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)(=[O:9])=[O:8]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A suspension of 1.18 g (0.004 mol) 2-(phenylsulfonyl)-ethanimidic acid ethyl ester hydrochloride in 15 ml chloroform was treated with 6 ml 1N aqueous sodium hydoxide. The mixture was extracted with dichloromethane. The extracts were combined and dried with magnesium sulfate and the solvents were distilled off under reduced pressure. The resulting colorless oil was stirred together with 0.68 g (0.004 mol) 4,5-dimethyl-furan-2-carboxylic acid hydrazide in 10 ml chloroform for 24 hours at reflux temperature. Evaporation of the solvent and chromatography on silicagel with dichloromethane/methanol 19/1 gave 1.14 g (76%) 4,5-dimethyl-furan-2-carboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide as white crystals with mp. 197-199° C., MS m/e (%): 336 (M+H+, 100).
Aufarbeitung
- extractionThe mixture was extracted with dichloromethane
- dry with materialdried with magnesium sulfate
- distillationthe solvents were distilled off under reduced pressure
- temperatureat reflux temperature
- customEvaporation of the solvent and chromatography on silicagel with dichloromethane/methanol 19/1
Quellen und Nachweise
- ORD-Eintrag
- ord-6307b44407084017a86a0455aed26e3f
- Quelldatensatz
- uspto-grants-2002_03
- Patentnummer
- US06355653B1
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