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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639686Generated: October 31, 2026

1-Azido-4-methoxybenzene → 5-(2,4-Dichlorophenyl)-3-(4-methoxyphenyl)triazol-4-amine

https://huagongshe.com/reaction/1639686

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Azido-4-methoxybenzeneHCID 75004—
Reactant2,4-DichlorophenylacetonitrileHCID 80566—
ReactantSodium MethoxideHCID 10942334—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product5-(2,4-Dichlorophenyl)-3-(4-methoxyphenyl)triazol-4-amineHCID 2521544325.4%

Reaction Steps

To an ice-cooled and stirred mixture of 1-azido-4-methoxy-benzene (0.750 g, 1 eq) and commercial (2,4-dichloro-phenyl)-acetonitrile (1.12 g, 1.2 eq) in ethanol (10 ml) kept under nitrogen, a solution of sodium methoxide (0.408 g, 1.5 eq) in ethanol (10 ml) is added drop-wise (25 min). After the addition, the reaction mixture is allowed to reach room temperature spontaneously and stirring is then continued overnight at room temperature. The resulting reaction mixture is diluted with ethyl acetate (40 ml), washed with water (2×50 ml), dried over MgSO4 and evaporated to dryness. The yellow semisolid residue (0.842 g) is purified by flash chromatography using 60-120 mesh silica gel and eluting with 15% ethylacetate in hexane, to afford the title compound as a white solid (0.428 g, 24% yield). M.p. 154.6-163.9° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110588B2
Source datasetuspto-grants-2012_02
ORD IDord-67709d0011cb4a1bbcc068801243af2c
Source noteuspto-grants-2012_02