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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491892Generated: October 30, 2026

Acetonitrile → methyl 1-benzyl-1H-1,2,4-triazole-3-carboxylate

https://huagongshe.com/reaction/491892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactantmethyl 1H-1,2,4-triazole-1-carboxylateHCID 642208—
Productmethyl 1-benzyl-1H-1,2,4-triazole-3-carboxylateHCID 67023628—

Reaction Steps

A solution of methyl 1,2,4-triazole-2-carboxylate (6.89 g, 54.2 mmole), benzyl bromide (7.7 mL, 65.0 mmol) and potassium carbonate (11.24 g, 81.3 mmol) in acetonitrile (100 mL) was refluxed overnight. The solution was then filtered and concentrated to a residue. The residue was dissolved in diethyl ether. The solution washed with 1N sodium hydroxide one time and water one time, and then dried over MgSO4. The solution was filtered and concentrated to yield 1-benzyl-1H-[1,2,4]triazole-3-carboxylic acid methyl ester as a brown oil, which was used in next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531545B2
Source datasetuspto-grants-2009_05
ORD IDord-3f7ccd8f78dc45109610f39641ee36b2
Source noteuspto-grants-2009_05