HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283383Generated: October 30, 2026
Dimethylformamide → 7-Bromo-2-chloroquinoxaline
https://huagongshe.com/reaction/2283383
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 7-bromo-1H-quinoxalin-2-one | HCID 4913264 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-Bromo-2-chloroquinoxaline | HCID 4913253 | 74.7% |
Reaction Steps
Thionyl chloride (407.5 mL; 5.59 mol), then N,N-dimethylformamide (34.6 mL; 0.45 mol) were added dropwise to a mixture of 7-bromo-2(1H)-quinoxalinone (500 g; 2.24 mol) in toluene (7.61 L). The reaction mixture was stirred at 80° C. for 17 hours then cooled to 35° C. and poured cautiously onto water. The bi-phasic mixture was stirred for 30 minutes and then decanted. The organic layer was evaporated to dryness and the residue crystallized in methyl-tert-butyl ether, filtered and the precipitate washed with methyl-tert-butyl ether and dried to give 407 g (74.7%) of 7-bromo-2-chloro-quinoxaline. Filtrate was evaporated and re-crystallized in methyl-tert-butyl ether to provide a second fraction of 72 g (13.2%) of 7-bromo-2-chloro-quinoxaline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145394B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-ca197bd1d45d4975bccb945fa45080fa |
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| Source note | uspto-grants-2015_09 |
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