Reaktionsgleichung
[CH3:1][S:2](Cl)(=[O:4])=[O:3].[NH:6]1[CH2:10][CH:9]=[CH:8][NH:7]1.C(N(CC)CC)C>C(Cl)Cl>[CH3:1][S:2]([N:7]1[CH2:8][CH:9]=[CH:10][NH:6]1)(=[O:4])=[O:3]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
114.5 g of methanesulphonic acid chloride were added dropwise to 70 g of pyrazoline and 101 g of triethylamine in 300 ml of methylene chloride at room temperature. The mixture was subsequently stirred at room temperature for 3 hours and was filtered. The filtrate was washed with water, dried over sodium sulphate and concentrated. 114 g (77% of theory) of methanesulphonylpyrazoline of melting point 62° C. were obtained.
Aufarbeitung
- filtrationwas filtered
- washThe filtrate was washed with water
- dry with materialdried over sodium sulphate
- concentrationconcentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-a07ead0b1aaa4c1bb2f33c4ae7d2feac
- Quelldatensatz
- uspto-grants-1983_12
- Patentnummer
- US04423225
Verknüpfte Notizen
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