Phosphorus oxychloride → 2-(1-Bromoethyl)-3-chloro-6-fluoroquinoxaline
Reaktionsgleichung
[Br:1][CH:2]([C:4]1[C:5](=O)[NH:6][C:7]2[C:12]([N:13]=1)=[CH:11][CH:10]=[C:9]([F:14])[CH:8]=2)[CH3:3].P(Cl)(Cl)([Cl:18])=O>>[Br:1][CH:2]([C:4]1[C:5]([Cl:18])=[N:6][C:7]2[C:12](=[CH:11][CH:10]=[C:9]([F:14])[CH:8]=2)[N:13]=1)[CH3:3]Komponenten
Reaktionsbedingungen
- Temperatur
- 100 °C
Versuchsvorschrift
A heterogeneous mixture of 3-(1-bromoethyl)-7-fluoroquinoxalin-2(1H)-one (58.86 g, 217.1 mmol) and phosphorous oxychloride (198.8 ml, 2171 mmol) in a 1 L round bottom flask was stirred at 100° C. for 2 h. The mixture was hetereogeneous in the beginning of the reaction and then homogenesous black solution over 1 h. After 2 h, the mixture was cooled to rt and concentrated under reduced pressure. To the black residue was carefully added ice (˜400 ml) in portions and then water (200 ml) with stirring. The mixture was neutralized with NH4OH (200 ml) and ice (˜200 ml) with stirring. The resulting precipitate was collected by filtration, rinsed with water (1 L), and dried under high vacuum overnight to give 2-(1-bromoethyl)-3-chloro-6-fluoroquinoxaline (58.31 g, 92.8% yield) including 3-chloro-2-(1-chloroethyl)-6-fluoroquinoxaline as a brown solid.
Aufarbeitung
- customThe mixture was hetereogeneous in the beginning of the reaction
- waithomogenesous black solution over 1 h
- waitAfter 2 h
- temperaturethe mixture was cooled to rt
- concentrationconcentrated under reduced pressure
- stirringwater (200 ml) with stirring
- stirringwith stirring
- filtrationThe resulting precipitate was collected by filtration
- washrinsed with water (1 L)
- customdried under high vacuum overnight
Quellen und Nachweise
- ORD-Eintrag
- ord-7424f2ef061f47c09f709f93acabcff4
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08835432B2
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