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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019809Generated: October 30, 2026

1,3-Dibromo-5,5-dimethylhydantoin → 2-(1-Bromoethyl)-3,5-dichloroquinoxaline

https://huagongshe.com/reaction/1019809

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dibromo-5,5-dimethylhydantoinHCID 6479—
ReactantBenzoyl PeroxideHCID 7187—
Reactant3,5-Dichloro-2-ethylquinoxalineHCID 86698510—
SolventCarbon TetrachlorideHCID 5943—
Product2-(1-Bromoethyl)-3,5-dichloroquinoxalineHCID 86698511129%

Reaction Steps

3,5-Dichloro-2-ethylquinoxaline (1.10 Kg, 4.84 mol) was dissolved in CCl4 (4.4 L) at rt. 1,3-dibromo-5,5-dimethylhydantoin (762 g, 2.66 mol) and benzoyl peroxide (116 g, 0.48 mol) were then added. The resulting suspension was heated at reflux for 2 h. At this time LC-MS analysis showed that the reaction was complete. After cooling to rt white crystals formed in the reaction vessel. The white crystals were collected by filtration, washed with saturated aqueous NaHCO3 (3×5 L), and dried under high vacuum to give 2-(1-bromoethyl)-3,5-dichloroquinoxaline as a white solid (1.05 Kg). 1H NMR (DMSO-d6) δ ppm 8.04-8.12 (m, 2H), 7.78-7.90 (m, 1H), 5.76-5.84 (m, 1H), 2.09 (d, J=6.7 Hz, 3H). Mass Spectrum (ESI) m/z=304.8 [(M+1) (79Br)], 306.9 [(M+1) (81Br)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716290B2
Source datasetuspto-grants-2014_05
ORD IDord-bddd886454ef4a29a3aa054e356d2cbd
Source noteuspto-grants-2014_05