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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513339Generated: November 3, 2026

Hydrochloric Acid → 4-(Phenylcarbonyl)-1,2,4-triazine-3,5(2H,4H)-dione

https://huagongshe.com/reaction/1513339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
Reactant2-Acetyl-1,2,4-triazine-3,5(2H,4H)-dioneHCID 21256595—
Solvent1,4-DioxaneHCID 31275—
Product4-(Phenylcarbonyl)-1,2,4-triazine-3,5(2H,4H)-dioneHCID 1285011123.8%

Reaction Steps

To a solution of 2-acetyl-1,2,4-triazine-3,5(2H,4H)-dione (1.05 g, 6.77 mmol) in 1,4-dioxane (11 ml) and pyridine (1.64 ml, 20.31 mmol) was treated dropwise at 5° C. with benzoyl chloride (0.90 ml, 7.78 mmol), then the mixture was stirred at room temperature overnight. The day after, 0.1 eq of benzoyl chloride was added and the mixture was stirred at rt for further 4 hours. The reaction mixture was then filtered to remove the piridinium salt and the filtered was evaporated under vacuum. The residue was dissolved in ethanol (23 ml) and then hydrochloride acid 37% (0.74 ml, 24.19 mmol) was added and the reaction was refluxed for 15 minutes. The solvent was evaporated under reduced pressure and the residue was purified by column chromatography on silica eluting with a gradient of methanol in DCM (from 0 to 4%) to afford the title compound as a white solid (0.35 g, 23.47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217168B2
Source datasetuspto-grants-2012_07
ORD IDord-eb68c2debea54dcf90ed4ea2b939aa75
Source noteuspto-grants-2012_07