Reaktionsgleichung
[CH3:1][O:2][C:3](Cl)=[O:4].[CH3:6][S:7][CH2:8][CH2:9][O:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[NH:17][NH2:18].O>O1CCCC1.C(N(C(C)C)C(C)C)C>[CH3:1][O:2][C:3]([NH:18][NH:17][C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=1[O:10][CH2:9][CH2:8][S:7][CH3:6])=[O:4]Komponenten
6
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 20 °C
Versuchsvorschrift
5.6 ml of chloroformic acid methyl ester are added dropwise at 0° C. to 14.4 g of 2-(2-methylthioethoxy)-phenylhydrazine in 100 ml of tetrahydrofuran and 14 g of N-ethyldiisopropylamine. The reaction mixture is stirred at 20° C. for 2 hours; H2O is then added, and the mixture is repeatedly extracted with ethyl acetate. After customary further processing, a solid is obtained, and this is recrystallised from alcohol to thus yield the compond of the formula ##STR62## having a melting point of 92°-94° C.
Aufarbeitung
- extractionthe mixture is repeatedly extracted with ethyl acetate
- customAfter customary further processing, a solid is obtained
- customthis is recrystallised from alcohol
- customto thus yield the compond of the formula
Quellen und Nachweise
- ORD-Eintrag
- ord-e8648a916c7c4fcfb8175365162e18a3
- Quelldatensatz
- uspto-grants-1988_02
- Patentnummer
- US04725302
Verknüpfte Notizen
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