HCID 178478181, Verbindung → HCID 178478548, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[C:3]([C:7]2[CH:12]=[C:11]([Cl:13])[CH:10]=[C:9]([Cl:14])[CH:8]=2)=[N:4][NH:5][CH:6]=1>C(OCC)C>[ClH:1].[Cl:1][C:2]1[C:3]([C:7]2[CH:8]=[C:9]([Cl:14])[CH:10]=[C:11]([Cl:13])[CH:12]=2)=[N:4][NH:5][CH:6]=1.[Cl:1][C:2]1[C:3]([C:7]2[CH:8]=[C:9]([Cl:14])[CH:10]=[C:11]([Cl:13])[CH:12]=2)=[N:4][NH:5][CH:6]=1Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2 g (0.008 mol) of 4-chloro-3-(3,5-dichlorophenyl)pyrazole are dissolved, at room temperature and with stirring, in 200 ml of diethyl ether. Sparging with hydrochloric acid is then carried out until precipitation has ended. The white solid is filtered and rinsed with ether to give 1.1 g (yield 52%, melting point: 175° C.) of 4-chloro-3-(3,5-dichlorophenyl)pyrazole hemihydrochloride.
Aufarbeitung
- customSparging with hydrochloric acid
- customis then carried out until precipitation
- filtrationThe white solid is filtered
- washrinsed with ether
Quellen und Nachweise
- ORD-Eintrag
- ord-08857daf80a943b09997e599523ac755
- Quelldatensatz
- uspto-grants-1999_08
- Patentnummer
- US05945382
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