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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 75384Erstellt: 24. Oktober 2026

Carbon Tetrachloride → 3-(1-bromoethyl)-7-fluoroquinoxalin-2(1H)-one

https://huagongshe.com/de/reaction/75384

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon TetrachlorideHCID 5943—
Edukt1,3-Dibromo-5,5-dimethylhydantoinHCID 6479—
EduktBenzoyl PeroxideHCID 7187—
EduktSodium BicarbonateHCID 516892—
Edukt3-ethyl-7-fluoroquinoxalin-2(1H)-oneHCID 67289205—
Produkt3-(1-bromoethyl)-7-fluoroquinoxalin-2(1H)-oneHCID 86698519133%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

3-Ethyl-7-fluoroquinoxalin-2(1H)-one (20.61 g, 107.2 mmol) and 1,3-dibromo-5,5-dimethylhydantoin (18.77 g, 64.34 mmol) suspended in carbon tetrachloride (1072 ml, 107.2 mmol). To the heterogeneous mixture was added benzoyl peroxide (3.463 g, 10.72 mmol) and the mixture was heated at reflux with stirring (oil bath temperature: 80° C.) for 20 h. After 20 h, the mixture was cooled to rt. After cooling, the mixture was poured into saturated aqueous sodium bicarbonate solution (1 L) with stirring. The precipitate was collected by filtration and washed with water (1 L) to give 3-(1-bromoethyl)-7-fluoroquinoxalin-2(1H)-one (23.19 g, 79.8% yield) as a tan solid:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835432B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-92849659d0874c5281220a124d720487
Quellennotizuspto-grants-2014_09