HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232558Generated: November 3, 2026
Butyl bromide → 4-butyl-2H-[1,2,4]triazine-3,5-dione
https://huagongshe.com/reaction/232558
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Acetyl-1,2,4-triazine-3,5(2H,4H)-dione | HCID 21256595 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-butyl-2H-[1,2,4]triazine-3,5-dione | HCID 15229542 | 51.5% |
Reaction Steps
To a 50% sodium hydride suspension (4.8 g) in DMF (100 ml), compound 11a (15.5 g) dissolved in DMF (200 ml) is added drop by drop, maintaining the temperature at room temperature. After agitation for 2 hours, bromobutane (20 g) is added and the agitation continued for 12 hours. The reaction mixture is concentrated to dryness under vacuum at 60° C., taken up in water, and then extracted with methylene chloride. After concentration to dryness under vacuum, the oil is taken up in ethanol (100 ml), whereupon p-toluene-sulfonic acid (2 g) is added. After heating under reflux for 2 hours and leaving at room temperature for 12 hours, the reaction mixture is filtered. The precipitate is washed with an aqueous solution of sodium bicarbonate and water, and then dried in an oven under vacuum in order to give the compound 11b (8.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05591743 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-6974236b42d44bc78784a6372609c773 |
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| Source note | uspto-grants-1997_01 |
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