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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640694Generated: October 30, 2026

Ethanedioyl dibromide → HCID 58432792, compound

https://huagongshe.com/reaction/1640694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanedioyl dibromideHCID 84841—
ReactantHCID 59564946HCID 59564946—
CatalystDimethylformamideHCID 6228—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 58432792HCID 5843279293%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114881B2
Source datasetuspto-grants-2012_02
ORD IDord-3d83cc1120bf4238bf880e47ad1adaa7
Source noteuspto-grants-2012_02