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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 2-Acetyl-1,2,4-triazine-3,5(2H,4H)-dione | HCID 21256595 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(Phenylcarbonyl)-1,2,4-triazine-3,5(2H,4H)-dione | HCID 12850111 | 23.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08217168B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-eb68c2debea54dcf90ed4ea2b939aa75 |
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| Source note | uspto-grants-2012_07 |
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