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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737859Generated: October 26, 2026

4-(1,2,4-Triazol-1-ylmethyl)benzonitrile → 1-[1-(4-Cyanophenyl)-4-(4-fluorophenyl)butyl]-1,2,4-triazole

https://huagongshe.com/reaction/1737859

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1,2,4-Triazol-1-ylmethyl)benzonitrileHCID 7537616—
Reactant1-(3-Bromopropyl)-4-fluorobenzeneHCID 14737133—
ReactantButyllithiumHCID 178418339—
Product1-[1-(4-Cyanophenyl)-4-(4-fluorophenyl)butyl]-1,2,4-triazoleHCID 10758038—

Reaction Steps

The compound is prepared by the method described in Example 1 starting from 1-(4-cyanobenzyl)-1,2,4-triazole (6.0 g, 0.0272 mol), n-BuLi (0.0272 mol) and 3-(4-fluorophenyl)propylbromide (7.6 g, 0.035 mol). The product is purified first by suspending the residue with 2 M aqueous hydrogen chloride and petrol ether. Petrol ether phase is separated and the aqueous layer and the separated oil are extracted with diethyl ether. Diethyl ether phase is evaporated and the residue is purified by flash chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962495
Source datasetuspto-grants-1999_10
ORD IDord-670431ad6d644362ad564db62466aa3c
Source noteuspto-grants-1999_10