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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166416Generated: October 27, 2026

1H-1,2,4-Triazole → 1-(1H-1,2,4-triazol-1-yl)-2-isopropoxy-2-(2,4-dichlorophenyl)pentane

https://huagongshe.com/reaction/2166416

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantTriphenylphosphineHCID 11776—
ReactantAzodicarboxylic acid dimethyl esterHCID 351621—
Reactant2-(2,4-Dichlorophenyl)-2-isopropoxypentan-1-olHCID 23039713—
SolventTetrahydrofuranHCID 8028—
Product1-(1H-1,2,4-triazol-1-yl)-2-isopropoxy-2-(2,4-dichlorophenyl)pentaneHCID 23039686—

Reaction Steps

A solution of 5.5 g (30 mmoles) of dimethyl azodicarboxylate is added dropwise, at room temperature, to a solution of 5.8 g (20 mmoles) of 2-(2,4-dichlorophenyl)-2-isopropoxypentan-1-ol, 7.9 g (30 mmoles) of triphenylphosphine and 1.66 g (24 mmoles) of 1,2,4-triazole in 100 ml of absolute tetrahydrofuran, and the reaction mixture is then stirred for 3 hours at room temperature and then for a further 16 hours at 50° C. and is evaporated; the residue is digested with 100 ml of diethyl ether, the insoluble residue is filtered off, and the ether phase is concentrated again and purified by column chromatography (silica gel; 1:1 ethyl acetate/petroleum ether). This gives a colourless oil having physical data which agree entirely with those in Example 3b).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04945100
Source datasetuspto-grants-1990_07
ORD IDord-a1dba695f8394a7299a3bd7fff9ac90f
Source noteuspto-grants-1990_07