HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640694Generated: October 30, 2026
Ethanedioyl dibromide → HCID 58432792, compound
https://huagongshe.com/reaction/1640694
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanedioyl dibromide | HCID 84841 | — |
| Reactant | HCID 59564946 | HCID 59564946 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 58432792 | HCID 58432792 | 93% |
Reaction Steps
6-Methyl-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyrazine-2,3-dione (0.52 g, 1.92 mmol) and 1,2-dichloroethane (10 ml) were placed in a vial (20 ml). To the resulting suspension was added carefully oxalyl bromide (0.53 ml, 1.24 g, 5.75 mmol). A foam was formed during the addition, and as the foam was settling down the stirring was started. DMF (3 drops) was added and the vial was sealed and the mixture was stirred overnight. Another portion of oxalyl bromide (0.2 ml, 0.46 g, 2.23 mmol) and DMF (3 drops) was added and the reaction was run for another 24 h. The mixture was partitioned between DCM (20 ml) and water (20 ml) and the organic phase was dried. Filtration and evaporation gave a crude product, which was purified on silica, affording 0.59 g (93%) of 3-bromo-6-methyl-1-[3-(trifluoromethyl)phenyl]pyrazin-2(1H)-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08114881B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-3d83cc1120bf4238bf880e47ad1adaa7 |
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| Source note | uspto-grants-2012_02 |
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