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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962778Generated: October 31, 2026

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

https://huagongshe.com/reaction/962778

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 numberUS05760058
Source datasetuspto-grants-1998_06
ORD IDord-b33dd683fa5741a99375809a84768d1b
Source noteuspto-grants-1998_06