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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453645Generated: October 30, 2026

Methanol → 2-(4-Chloro-butyl)-2H-[1,2,4]triazine-3,5-dione

https://huagongshe.com/reaction/453645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1-Bromo-4-chlorobutaneHCID 81364—
Reactant1,2,4-Triazine, 3,5-bis[(trimethylsilyl)oxy]-HCID 87057—
CatalystIodineHCID 807—
Solvent1,1-DichloroethaneHCID 6365—
Product2-(4-Chloro-butyl)-2H-[1,2,4]triazine-3,5-dioneHCID 1581717576.5%

Reaction Steps

22.1 g of 3,5-Bis-trimethylsilanyloxy-[1,2,4]triazine (86 mmol) were dissolved in 150 mL of dichloroethane followed by addition of 14.7 g of 1-bromo-4-chloro-butane (86 mmol) and 0.218 g of iodine (0.858 mmol). The reaction mixture was stirred for 25 h at room temperature. Then, 300 mL of methanol were added and the mixture was stirred for an additional 10 minutes. The solvents were evaporated under reduced pressure and the residue was partitioned between dichloromethane and water. The aqueous phase was extracted several times with dichloromethane. The combined organic layers were washed with 10% aqueous sodium bicarbonate solution and saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered, and the organic phase was evaporated under reduced pressure. The thus obtained crude product was purified via silica gel chromatography using dichloromethane-methanol 0-10% to yield 13.4 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492540B2
Source datasetuspto-grants-2013_07
ORD IDord-53ded76454e04703a7aef4522fde93ca
Source noteuspto-grants-2013_07