Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257140Generated: November 1, 2026

1H-1,2,4-Triazole → Benzyl 4-(1,2,4-triazol-1-yl)butyrate

https://huagongshe.com/reaction/2257140

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzyl 4-bromobutanoateHCID 3832489—
SolventAcetonitrileHCID 6342—
ProductBenzyl 4-(1,2,4-triazol-1-yl)butyrateHCID 1049057981.1%

Reaction Steps

4.7 g of 1,2,4-triazole and 9.5 g of potassium carbonate were added to a solution of 15 g of benzyl 4-bromobutyrate in 150 ml of acetonitrile. The mixture was refluxed by heating, for 1 hour. The reaction mixture was concentrated under reduced pressure. To the residue was added 30 ml of methylene chloride. The insolubles were collected by filtration and washed. The filtrate and the washings were combined and purified by silica gel column chromatography (eluant: methylene chloride/methanol=50/1) to obtain 11.6 g of benzyl 4-(1,2,4-triazol-1-yl)butyrate as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05656642
Source datasetuspto-grants-1997_08
ORD IDord-841fdb412580443ba1fdd649fef8d35b
Source noteuspto-grants-1997_08