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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883628Generated: November 1, 2026

Lithium Hydroxide → 5-difluoromethyl-2-methyl-4-(2-methyl-5-phenylbenzyl)-2,4-dihydro-3H-1,2,4-triazol-3-one

https://huagongshe.com/reaction/1883628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantSodium IodideHCID 5238—
Reactant2-Methyl-5-phenylbenzyl chlorideHCID 23508229—
Reactant5-(Difluoromethyl)-2-methyl-1H-1,2,4-triazol-3(2H)-oneHCID 135838251—
SolventTolueneHCID 1140—
Product5-difluoromethyl-2-methyl-4-(2-methyl-5-phenylbenzyl)-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 12056521—
Product3-difluoromethyl-1-methyl-5-(2-methyl-5-phenylbenzyloxy)-1H-1,2,4-triazoleHCID 23508214—

Reaction Steps

A mixed suspension of 69 mg (0.461 mmol) of 5-difluoromethyl-2-methyl-2,4-dihydro-3H-1,2,4-triazol-3-one (produced in the same manner as in Intermediate Production Example), 12 mg (0.508 mmol) of lithium hydroxide, 14 mg (0.092 mmol) of sodium iodide and 3 ml of toluene was stirred for 2 hours while heating under reflux. Toluene was distilled off under reduced pressure, 3 ml of anhydrous 1,4-dioxane was added to the residue under nitrogen atmosphere, then, 100 mg (0.461 mmol) of 2-methyl-5-phenylbenzyl chloride was added. The reaction solution was stirred for 18 hours while heating under reflux, then, concentrated. Ethyl acetate was added to the residue, the mixture was washed with water, then, washed with saturated saline, and dried over anhydrous magnesium sulfate, then, concentrated. The residue was subjected to silica gel thin layer chromatography (eluant: hexane/ethyl acetate=3/1 (v/v)), to obtain 61 mg of 5-difluoromethyl-2-methyl-4-(2-methyl-5-phenylbenzyl)-2,4-dihydro-3H-1,2,4-triazol-3-one (Compound 1) and 11 mg of 3-difluoromethyl-1-methyl-5-(2-methyl-5-phenylbenzyloxy)-1H-1,2,4-triazole as a by-product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06762197B2
Source datasetuspto-grants-2004_07
ORD IDord-7914c2f9fc804d65bfc0b314e8603f6c
Source noteuspto-grants-2004_07