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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729271Generated: October 30, 2026

Acetonitrile → 1-(4-methylphenyl)-2-(1h-1,2,4-triazol-1-yl)ethanone

https://huagongshe.com/reaction/1729271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant2-Bromo-4'-methylacetophenoneHCID 69272—
ReactantHCID 178507080HCID 178507080—
Product1-(4-methylphenyl)-2-(1h-1,2,4-triazol-1-yl)ethanoneHCID 739371—

Reaction Steps

2-Bromo-4'-methylacetophenone (12.78 g; 0.06 mole), sodium triazole (5.46 g; 0.06 mole) in dry acetonitrile solution (100 ml) were stirred at 20° C. for 5 hours. The solvent was evaporated and the residue purified by chromatography using silica gel/chloroform to give 2-(1,2,4-triazol-1- yl)-4'-methylacetophenone as a white solid (mp 118.4° C.). The latter compound (3.0 g; 0.015 mole) together with sodium acetate (1.23 g; 0.015 mole) and acetic acid (30 ml), was stirred at 40° C. during the addition of bromine (2.38 g; 0.015 mole) in acetic acid (2 ml). The mixture was stirred for a further 30 minutes and poured into chloroform (50 ml) and washed with water and sodium bicarbonate solution. The chloroform layer was separated, dried (MgSO4) and evaporated to give crude 2-bromo-2-(1,2,4-triazol-1-yl)-4'-methylacetophenone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05332753
Source datasetuspto-grants-1994_07
ORD IDord-64e0abc5f9724e07ac5ce3349688875d
Source noteuspto-grants-1994_07