Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359139Generated: October 30, 2026

Water → HCID 14537614, compound

https://huagongshe.com/reaction/359139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 14537612HCID 14537612—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 14537614HCID 1453761461.9%

Reaction Steps

A solution of 20.5 g (0.077 mol) of 2-(4-chlorophenylethyl)-2-(1,1-dimethylbutyl)-oxirane, 5.3 g (0.077 mol) of 1,2,4-triazole, 1.0 g (0.025 mol) of sodium hydroxide, 1 ml of water and a spatula tipful of α,α'-azoisobutyronitrile in 50 ml of N-methylpyrrolidone is heated at 120° C. for 5 hours. After this, the solution is cooled to room temperature and concentrated by stripping off the solvent under reduced pressure, the remaining residue is dissolved in acetic acid 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=4:1). In this manner 16.0 g (61.9% of theory) of 1-(4-chlorophenyl)-4,4-dimethyl-3-(1,2,4-triazol-1-yl-methyl)-3-heptanol are obtained in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04999440
Source datasetuspto-grants-1991_03
ORD IDord-0ba939332c844e8c85de6e1ddf4917f8
Source noteuspto-grants-1991_03