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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352059Generated: October 30, 2026

Sodium Iodide → 2-Benzyl-1,2,3-triazole

https://huagongshe.com/reaction/352059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178418936HCID 178418936—
SolventTolueneHCID 1140—
Solvent2-Methyl-2-butanolHCID 6405—
Product1-Benzyl-1,2,3-triazoleHCID 138203—
Product2-Benzyl-1,2,3-triazoleHCID 53254676%

Reaction Steps

1,2,3-Triazole (1523 mg, 22.05 mmol), sodium iodide (2203 mg, 14.7 mmol) and sodium hydroxide (882 mg, 22.05 mmol) were added to t-amyl alcohol (5.8 ml), and the mixture was refluxed under stirring for 1 hour. Benzyl chloride (1861 mg, 14.7 mmol) was dissolved in t-amyl alcohol (5.8 ml) and added dropwise under reflux over 1 hour. The mixture was refluxed under stirring for 1 hour. The mixture was cooled to room temperature and toluene (50 ml) was added. The mixture was washed with water (50×2), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=3/1→1/3) to give 1-benzyl-1H-1,2,3-triazole (2.10 g) as white crystals, yield 90%, and 2-benzyl-2H-1,2,3-triazole (140 mg) as white crystals (yield 6%). 1-benzyl-1H-1,2,3-triazole

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743924B2
Source datasetuspto-grants-2004_06
ORD IDord-0ce0019280cb4a238e5e3f72338e79a9
Source noteuspto-grants-2004_06