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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dichlorobenzyl chloride | HCID 7212 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 20574477 | HCID 20574477 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 23335431 | HCID 23335431 | 33.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04229459 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-81e7ffa6816744df90626a6bf1890450 |
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| Source note | uspto-grants-1980_10 |
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