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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dibromo-5,5-dimethylhydantoin | HCID 6479 | — |
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | 3,5-Dichloro-2-ethylquinoxaline | HCID 86698510 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(1-Bromoethyl)-3,5-dichloroquinoxaline | HCID 86698511 | 129% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08835432B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-e14931c3a7b54cd7b280a4c2b71c8589 |
|---|
| Source note | uspto-grants-2014_09 |
|---|