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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75373Generated: October 30, 2026

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

https://huagongshe.com/reaction/75373

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 numberUS08835432B2
Source datasetuspto-grants-2014_09
ORD IDord-e14931c3a7b54cd7b280a4c2b71c8589
Source noteuspto-grants-2014_09