HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087698Generated: October 30, 2026
1H-1,2,4-Triazole → 2-(4-Chlorophenoxymethyl)-1-(1,2,4-triazol-1-yl)-3,3,4-trimethylpentan-2-ol
https://huagongshe.com/reaction/1087698
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | 2-(4-Chlorophenoxymethyl)-2-(1,1,2-trimethylpropyl)-oxirane | HCID 22163227 | — |
| Reactant | Sodium n-butylate | HCID 23669364 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 2-(4-Chlorophenoxymethyl)-1-(1,2,4-triazol-1-yl)-3,3,4-trimethylpentan-2-ol | HCID 14328585 | 36.8% |
Reaction Steps
376 g of crude 2-(4-chlorophenoxymethyl)-2-(1,1,2-trimethylpropyl)-oxirane dissolved in 400 ml of n-butanol are added dropwise to a boiling solution of 13.4 g (0.14 mol) of sodium butanolate and 97 g (1.4 mols of 1,2,4-triazole in 400 ml of n-butanol in 1.5 hours. After boiling under reflux for 22 hours, the solvent is removed by distillation under reduced pressure and 500 ml of dichloromethane are added to the residue. Precipitated 2-(4-chlorophenoxymethyl)-1-(1,2,4-triazol-4-yl)-3,3,4-trimethylpentan-2-ol (15 g; melting point 173°-174° C.) is filtered off from the mixture, the filtrate is washed twice with 250 ml of water each time and dried over anhydrous sodium sulphate and the solvent is removed by distillation. The residue is chromatographed on silica gel using trichloromethane as eluant. 174 g of 2-(4-chlorophenoxymethyl)-1-(1,2,4-triazol-1-yl)-3,3,4-trimethylpentan-2-ol are thus obtained in the form of colorless crystals of melting point 59°-60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04960453 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-c0e201cccb794cf1a748d66ff1d24459 |
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| Source note | uspto-grants-1990_10 |
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