Reaktionsgleichung
[O:1]=[C:2]1[NH:7][C:6]([C:8]([F:14])([F:13])[C:9]([F:12])([F:11])[F:10])=[C:5]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH2:4][CH2:3]1.BrN1C(=O)CCC1=O>C(Cl)(Cl)(Cl)Cl>[O:1]=[C:2]1[NH:7][C:6]([C:8]([F:13])([F:14])[C:9]([F:10])([F:11])[F:12])=[C:5]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH:4]=[CH:3]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 80 °C
Versuchsvorschrift
A suspension of ethyl 6-oxo-2-(pentafluoroethyl)-1,4,5,6-tetrahydropyridine-3-carboxylate (0.690 g) and N-bromosuccinimide (0.427 g) in carbon tetrachloride (5 mL) was heated at 80° C. for 20 h. The reaction mixture was concentrated in vacuo and subjected to flash column chromatography (eluent 1:3 ethyl acetate/isohexane) to yield a colourless solid (0.30 g).
Aufarbeitung
- concentrationThe reaction mixture was concentrated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-885a408ad58b46549dc94731e4f37375
- Quelldatensatz
- uspto-grants-2011_06
- Patentnummer
- US07956070B2
Verknüpfte Notizen
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