Reaktionsgleichung
[NH2:1][C:2]1[C:3]([F:10])=[CH:4][C:5]([Cl:9])=[C:6]([OH:8])[CH:7]=1.Cl.[N:12]([O-])=O.[Na+].[Sn](Cl)Cl>O.S(=O)(=O)(O)O>[ClH:9].[F:10][C:3]1[CH:4]=[C:5]([Cl:9])[C:6]([OH:8])=[CH:7][C:2]=1[NH:1][NH2:12]Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
First, 32.3 g of 5-amino-2-chloro-4-fluorophenol was mixed with 150 ml of concentrated hydrochloric acid, and the mixture was stirred at 50° C. for 30 minutes, to which a solution of 15 g of sodium nitrite dissolved in 40 ml of water was added dropwise at 0° C. over 10 minutes. After stirring at 0° C. for 1 hour, the mixture was cooled to -50° C. Then, a solution of 132 g of tin (II) chloride dissolved in 132 g of concentrated sulfuric acid was rapidly added dropwise at -50° C., and the mixture was gradually warmed to room temperature and stirred for 1 hour. The solids formed were collected by filtration and dried at 80° C. under reduced pressure to give 75 g of the crude 2-fluoro-4-chloro-5-hydroxyphenylhydrazine hydrochloride crystals.
Aufarbeitung
- additionwas added dropwise at 0° C. over 10 minutes
- temperaturethe mixture was cooled to -50° C
- additionwas rapidly added dropwise at -50° C.
- temperaturethe mixture was gradually warmed to room temperature
- stirringstirred for 1 hour
- customThe solids formed
- filtrationwere collected by filtration
- customdried at 80° C. under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-32abd69c63984df281faf9fc48596faa
- Quelldatensatz
- uspto-grants-2000_07
- Patentnummer
- US06090753
Verknüpfte Notizen
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