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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271412Generated: November 3, 2026

Potassium Iodide → 1-[3-(4-nitro-phenoxy)-propyl]-1H-[1,2,3]triazole

https://huagongshe.com/reaction/1271412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium HydroxideHCID 14798—
Reactant1-(3-Chloropropoxy)-4-nitrobenzeneHCID 11844617—
ReactantHCID 178418936HCID 178418936—
Solvent2-Methyl-2-butanolHCID 6405—
Product1-[3-(4-nitro-phenoxy)-propyl]-1H-[1,2,3]triazoleHCID 18453518—

Reaction Conditions

Temperature120 °C

Reaction Steps

1-(3-Chloro-propoxy)-4-nitro-benzene (7 g, 32.5 mmol) is dissolved in 2-methyl-2-butanol (35 ml) followed by the addition of 1H-1,2,3-triazole (3.43 g, 48.7 mmol), potassium iodide (0.54 g, 3.25 mmol) and sodium hydroxide (1.95 g, 48.7 mmol). The mixture is stirred for 20 h at 120° C., evaporated to dryness and suspended in toluene. Washing with water, drying over sodium sulfate and concentration in vacuo yields a crude product, which is washed with ether yielding 1-[3-(4-nitro-phenoxy)-propyl]-1H-[1,2,3]triazole as a colorless solid. Yield 6 g (75%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205326B2
Source datasetuspto-grants-2007_04
ORD IDord-f4d1b83b68d740f3ba350f72807f270d
Source noteuspto-grants-2007_04