Reaktionsgleichung
[CH3:1][C:2](/[CH:4]=[N:5]/[OH:6])=O.Cl.[F:8][C:9]1[CH:14]=[CH:13][C:12]([NH:15][NH2:16])=[CH:11][CH:10]=1>C(OCC)C.O.O.O.O.O.O.S([O-])([O-])(=O)=O.[Cu+2]>[F:8][C:9]1[CH:14]=[CH:13][C:12]([N:15]2[N:16]=[C:2]([CH3:1])[CH:4]=[N+:5]2[O-:6])=[CH:11][CH:10]=1Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Reaktionsbedingungen
- Temperatur
- 23 °C
Versuchsvorschrift
To a stirred solution of anti-pyruvic aldehyde 1-oxime (3.4 g, 39 mmol) in diethyl ether (75 mL) was added 4-fluorophenylhydrazine hydrochloride (5.85 g, 36 mmol). The reaction mixture was stirred at 23° C. for 16 h, and then concentrated under reduced pressure. The crude residue was dissolved in pyridine (120 mL). A solution of copper(II) sulfate pentahydrate (18 g, 72 mmol) in water (55 mL) was added dropwise over 4 min. The resulting mixture was stirred at reflux for 2 h. The mixture was concentrated under reduced pressure to remove excess pyridine. To the mixture was added 1.0 M aqueous hydrochloric acid. The mixture was extracted with ethyl acetate and the organic layer was separated and washed with 1.0 M aqueous hydrochloric acid until a clear amber organic layer was obtained. The organic layer was dried (MgSO4), filtered, and evaporated under reduced pressure to afford the title compound (6.6 g) as a colorless solid. The title compound was used directly in the next step without further purification.
Aufarbeitung
- concentrationconcentrated under reduced pressure
- dissolutionThe crude residue was dissolved in pyridine (120 mL)
- stirringThe resulting mixture was stirred
- temperatureat reflux for 2 h
- concentrationThe mixture was concentrated under reduced pressure
- customto remove excess pyridine
- additionTo the mixture was added 1.0 M aqueous hydrochloric acid
- extractionThe mixture was extracted with ethyl acetate
- customthe organic layer was separated
- washwashed with 1.0 M aqueous hydrochloric acid until a clear amber organic layer
- customwas obtained
- dry with materialThe organic layer was dried (MgSO4)
- filtrationfiltered
- customevaporated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-80c695a5e9c641f3a17b8e5a9a48124c
- Quelldatensatz
- uspto-grants-2016_04
- Patentnummer
- US09302999B2
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