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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639692Generated: October 25, 2026

Benzeneacetonitrile, 4-methoxy- → 3-(2-Fluoro-4-trifluoromethyl-phenyl)-5-(4-methoxy-phenyl)-3H-[1,2,3]triazol-4-ylamine

https://huagongshe.com/reaction/1639692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneacetonitrile, 4-methoxy-HCID 66031—
ReactantSodium MethoxideHCID 10942334—
Reactant1-Azido-2-fluoro-4-(trifluoromethyl)benzeneHCID 86645068—
SolventMethanolHCID 887—
Product3-(2-Fluoro-4-trifluoromethyl-phenyl)-5-(4-methoxy-phenyl)-3H-[1,2,3]triazol-4-ylamineHCID 252156771.7%

Reaction Steps

To a stirred and ice-cooled solution of sodium methoxide (1.659 g, 30.7146 mmol) in methanol (50 ml), 4-methoxyphenylacetonitrile (3.728 g, 24.5717 mmol) and 1-azido-2-fluoro-4-trifluoromethyl-benzene (4.200 g, 20.4764 mmol) are added portion wise and the mixture is allowed attain room temperature spontaneously and refluxed overnight. The resulting reaction mixture is concentrated, added water, and extracted with chloroform (3×100 mL). The combined organic layers are dried over MgSO4, filtered and concentrated to afford a brownish gummy material (5.900 g, 82% mass balance). The crude residue is purified by column chromatography over silica gel (230-400 mesh), eluting with 15% ethylacetate in hexane, to obtain the title compound as a grey solid (0.120 g, 1.5% yield). A major impurity isolated and characterized is 5-(4-methoxy-phenyl)-3-(2-methoxy-4-trifluoromethyl-phenyl)-3H-[1,2,3]triazol-4-ylamine (2.400 g, ˜33% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110588B2
Source datasetuspto-grants-2012_02
ORD IDord-848cecca055f4c178b53ca0a3eb22bdb
Source noteuspto-grants-2012_02