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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329952Generated: October 28, 2026

Water → HCID 20066175, compound

https://huagongshe.com/reaction/329952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 14537613HCID 14537613—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 20066175HCID 2006617547%

Reaction Steps

A solution of 89 g (0.352 mol) of 2-(4-chlorophenylethyl)-2-pentyl-oxirane, 26.5 g (0.384 mol) of 1,2,4-triazole, 3.5 g (0.0875 mol) of sodium hydroxide, 1.2 ml of water and a spatula tipful of α,α'-azoisobutyronitrile in 175 ml of N-methylpyrrolidone is heated at 120° C. for 4 hours. After this the mixture is cooled to room temperature and concentrated by stripping off the solvent under reduced pressure, the remaining residue is dissolved in ethyl acetate and washed three times with water, the organic phase is dried over sodium sulphate and the solvent is removed under reduced pressure. The residue is purified by column chromatography (silica gel; dichloromethane:ethyl acetate=1:1). In this manner 53.2 g (47.0% of theory) of 1-(4-chlorophenyl)-3-(1,2,4-triazol-1-yl-methyl)-3-octanol are obtained in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04894383
Source datasetuspto-grants-1990_01
ORD IDord-569a91f63a2646b08c2b53fcaf2b82ec
Source noteuspto-grants-1990_01