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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903901Generated: October 30, 2026

2,4-Dichlorobenzyl chloride → HCID 23335431, compound

https://huagongshe.com/reaction/903901

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichlorobenzyl chlorideHCID 7212—
ReactantSodium hydrideHCID 24758—
ReactantHCID 20574477HCID 20574477—
ReactantHCID 178418361HCID 178418361—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 23335431HCID 2333543133.1%

Reaction Steps

19.2 g (0.05 mol) of 1-(4-chlorophenoxy)-2-(2,4-dichlorophenyl)-1-(1,2,4-triazol-1-yl)-ethan-2-ol were dissolved in 100 ml of dioxane and the solution was added dropwise to a mixture of 2 g of 80% strength sodium hydride in 100 ml of dioxane at 80° C. After the evolution of hydrogen had subsided, 10 g (0.05 mol) of 2,4-dichlorobenzyl chloride were added dropwise and the mixture was heated under reflux for 15 hours. After cooling, the solvent was distilled off in vacuo and the residue was taken up in 100 ml of water and 100 ml of methylene chloride. The organic phase was separated off, washed twice with 100 ml of water each time, dried over sodium sulphate and concentrated by distilling off the solvent in vacuo. The solid residue was recrystallized from ether. 9 g (31% of theory) of 1-(4-chlorophenoxy)-2-(2,4-dichlorobenzyloxy)-2-(2,4-dichlorophenyl)-1-(1,2,4-triazol- 1-yl)-ethane of melting point 132°-135° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04229459
Source datasetuspto-grants-1980_10
ORD IDord-81e7ffa6816744df90626a6bf1890450
Source noteuspto-grants-1980_10