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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397806Generated: November 1, 2026

Carbon Tetrachloride → HCID 57707841, compound

https://huagongshe.com/reaction/1397806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
Reactant1,3-Dibromo-5,5-dimethylhydantoinHCID 6479—
ReactantBenzoyl PeroxideHCID 7187—
ReactantHCID 57707825HCID 57707825—
ProductHCID 57707841HCID 57707841—

Reaction Steps

3-(2-Chlorophenyl)-2-methyl-5-(trifluoromethyl)quinoxaline (0.9969 g, 3.089 mmol) and 1,3-dibromo-5,5-dimethylhydantoin (0.5299 g, 1.853 mmol) were suspended in carbon tetrachloride (30.89 mL, 3.089 mmol). To the mixture was added benzoyl peroxide (0.09977 g, 0.3089 mmol) and the mixture was heated at reflux. After 20 h, the mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by silica gel column chromatography on a 80 g of Redi-Sep™ column using 0 to 5% gradient of EtOAc in hexane over 10 min, then 5% isocratic of EtOAc for 30 min, then 5 to 20% gradient of EtOAc in hexane over 20 min, then 20% isocratic of EtOAc for 4 min as eluent to give 2-(bromomethyl)-3-(2-chlorophenyl)-5-(trifluoromethyl)-quinoxaline as an off-white syrupy solid: 1H NMR (400 MHz, DMSO-d6) δ ppm 8.48 (1 H, dd, J=8.6, 0.8 Hz), 8.37 (1 H, d, J=6.7 Hz), 8.09 (1 H, t, J=7.8 Hz), 7.55-7.77 (4 H, m), 4.73 (2 H, d, J=61.8 Hz); LC-MS (ESI) m/z 403.0 [M+11]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901135B2
Source datasetuspto-grants-2014_12
ORD IDord-e2798e55b1a049b1880b7982664511a2
Source noteuspto-grants-2014_12