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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085799Generated: October 26, 2026

1H-1,2,4-Triazole → 1,3-Bis(1H-1,2,4-triazol-1-yl)-2-(4-chlorophenyl)-3-methylbutan-2-ol

https://huagongshe.com/reaction/1085799

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantSodiumHCID 5360545—
Reactant4-Chlorophenyl-2-[2-(1,2,4-triazol-1-yl)-prop-2-yl]-oxiraneHCID 13366863—
Solvent1-PropanolHCID 1031—
Product1,3-Bis(1H-1,2,4-triazol-1-yl)-2-(4-chlorophenyl)-3-methylbutan-2-olHCID 1336686524.2%

Reaction Steps

3.6 g (0.052 mole) of 1,2,4-triazole are added to a solution of 0.11 g (0.047 mole) of sodium in 30 ml of n-propanol at room temperature, while stirring. The mixture is heated to the reflux temperature and a solution of 2-(4-chlorophenyl)-2-[2-(1,2,4-triazol-1-yl)prop-2-yl]-oxirane in 20 ml of n-propanol is added. The reaction mixture is heated under reflux for 15 hours and then cooled and poured onto water. The mixture is extracted with methylene chloride and the organic phase is dried over sodium sulphate and concentrated. The residue is purified by column chromatography (silica gel; chloroform:methanol=9:1). 3.7 g (24.2% of theory) of 2-(4-chlorophenyl)-1,3-di-(1,2,4-triazol-1-yl)-3-methyl-2-butanol of melting point 114° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011850
Source datasetuspto-grants-1991_04
ORD IDord-8eb319d7b0cc4f8dba883b0698216725
Source noteuspto-grants-1991_04