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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75384Generated: October 26, 2026

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

https://huagongshe.com/reaction/75384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
Reactant1,3-Dibromo-5,5-dimethylhydantoinHCID 6479—
ReactantBenzoyl PeroxideHCID 7187—
ReactantSodium BicarbonateHCID 516892—
Reactant3-ethyl-7-fluoroquinoxalin-2(1H)-oneHCID 67289205—
Product3-(1-bromoethyl)-7-fluoroquinoxalin-2(1H)-oneHCID 86698519133%

Reaction Conditions

Temperature80 °C

Reaction Steps

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:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835432B2
Source datasetuspto-grants-2014_09
ORD IDord-92849659d0874c5281220a124d720487
Source noteuspto-grants-2014_09