p-Toluenesulfonic acid → HCID 20367243, Verbindung
Reaktionsgleichung
C([O:3][C:4](=O)[CH:5]=[C:6]([NH2:10])OCC)C.C1(C)C=CC(S(O)(=O)=O)=CC=1.[Cl:23][C:24]1[CH:32]=[CH:31][C:30]([Cl:33])=[CH:29][C:25]=1[CH2:26][NH:27][NH2:28]>C(O)C>[NH2:10][C:6]1[NH:28][N:27]([CH2:26][C:25]2[CH:29]=[C:30]([Cl:33])[CH:31]=[CH:32][C:24]=2[Cl:23])[C:4](=[O:3])[CH:5]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
32.8 g of β-amino-β-ethoxyacrylic acid ethyl ester and 1 g of p-toluenesulphonic acid were dissolved in 120 ml of ethanol and 39 g of 2,5-dichlorobenzylhydrazine were added under nitrogen. After stirring for 2 hours the mixture was left to stand overnight and the compound identified above, which precipitated, was filtered off and recrystallised from ethanol. Melting point: 195°-196° C; Yield: 23 g (43%).
Aufarbeitung
- waitwas left
- waitto stand overnight
- customprecipitated
- filtrationwas filtered off
- customrecrystallised from ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-9cebfe5b38b34abc8a4f6fca571d5ba8
- Quelldatensatz
- uspto-grants-1978_02
- Patentnummer
- US04076943
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