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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352058Generated: November 3, 2026

Sodium Iodide → HCID 10702735, compound

https://huagongshe.com/reaction/352058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant2-ChloroacetophenoneHCID 10757—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178418936HCID 178418936—
SolventTolueneHCID 1140—
Solvent2-Methyl-2-butanolHCID 6405—
ProductHCID 10702735HCID 1070273545.2%

Reaction Steps

1,2,3-Triazole (1689 mg, 24.45 mmol), sodium iodide (2443 mg, 16.3 mmol) and sodium hydroxide (978 mg, 24.45 mmol) were added to t-amyl alcohol (6.5 ml), and the mixture was refluxed under stirring for 1 hour. 2-Chloro-1-phenylethanone (2520 mg, 16.3 mmol) was dissolved in t-amyl alcohol (13 ml) and added dropwise over 1 hour. The mixture was refluxed under stirring for 1 hour. The mixture was cooled to room temperature, toluene (50 ml) was added. The mixture was washed with water (50 ml×2), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=3/2→1/4) to give 1-phenyl-2-(1H-1,2,3-triazol-1-yl)ethanone (1.38 g) as brown crystals (yield 45%). 1-Phenyl-2-(2H-1,2,3-triazol-2-yl)ethanone (550 mg) was obtained as yellow crystals (yield 18%). 1-phenyl-2-(1H-1,2,3-triazol-1-yl)ethanone

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743924B2
Source datasetuspto-grants-2004_06
ORD IDord-6f289981d4a54f3d96b1acaacb001200
Source noteuspto-grants-2004_06