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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl bromideHCID 8002—
ReactantSodium hydrideHCID 24758—
Reactant2-Acetyl-1,2,4-triazine-3,5(2H,4H)-dioneHCID 21256595—
SolventDimethylformamideHCID 6228—
Product4-butyl-2H-[1,2,4]triazine-3,5-dioneHCID 1522954251.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05591743
Source datasetuspto-grants-1997_01
ORD IDord-6974236b42d44bc78784a6372609c773
Source noteuspto-grants-1997_01