Reaktionsgleichung
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[NH:9][NH:10][C:11]([O:13][CH2:14][CH2:15][Cl:16])=[O:12].[CH3:17][O:18][CH2:19][C:20](Cl)=[O:21].COCC(O)=O.S(Cl)(Cl)=O>C1(C)C(C)=CC=CC=1>[CH3:17][O:18][CH2:19][C:20]([N:9]([C:3]1[C:4]([CH3:8])=[CH:5][CH:6]=[CH:7][C:2]=1[CH3:1])[NH:10][C:11]([O:13][CH2:14][CH2:15][Cl:16])=[O:12])=[O:21]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
200 g (0.825 mol) 2-Chloroethyl 2-(2,6-dimethylphenyl)-hydrazinecarboxylate in 500 ml xylene are warmed to 80°, and added to a warm (80°) solution of 2-methoxyacetylchloride in 250 ml xylene, prepared in situ by treating 73.5 g (0.826 mol) 2-methoxyacetic acid in 250 ml xylene with 107.1 g (0.9 mol) thionyl chloride at 80° for 2 hours. The mixture is heated for 30 minutes at 80°, then worked up as described in Example 1a.
Aufarbeitung
- additionadded to
- customprepared in situ
- temperatureThe mixture is heated for 30 minutes at 80°
Quellen und Nachweise
- ORD-Eintrag
- ord-6096314213fa4998bf197d11be76b84e
- Quelldatensatz
- uspto-grants-1982_08
- Patentnummer
- US04347253
Verknüpfte Notizen
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