HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380921Generated: October 26, 2026
Water → 3-(4-Chlorophenoxy)-2-(4-chlorophenyl)-3-methyl-1-(1,2,4-triazol-1-yl)-2-butanol
https://huagongshe.com/reaction/1380921
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 2-[2-(4-Chlorophenoxy)propan-2-yl]-2-(4-chlorophenyl)oxirane | HCID 19842485 | — |
| Reactant | 1h-1,2,4-Triazole sodium salt | HCID 45489822 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | 3-(4-Chlorophenoxy)-2-(4-chlorophenyl)-3-methyl-1-(1,2,4-triazol-1-yl)-2-butanol | HCID 13217409 | 18.4% |
Reaction Steps
A solution of 30 g (0.093 mol) of 2-(4-chlorophenyl)-2-[2-(p-chlorophenoxy)-prop-2-yl]-oxirane in 40 ml of n-propanol is added dropwise to a solution of 7.6 g (0.107 mol) of sodium 1,2,4-triazole in 60 ml of n-propanol at room temperature. The reaction mixture is subsequently stirred at the reflux temperature for 48 hours and is cooled, water is added and the mixture is extracted with methylene chloride. The organic phase is dried over sodium sulphate and concentrated in vacuo. The oily residue is purified by column chromatography. 6.7 g (18.4% of theory) of 3-(4-chlorophenoxy)-2-(4-chlorophenyl)-3-methyl-1-(1,2,4-triazol-1-yl)-2-butanol are obtained. This product is stirred with 20 ml of saturated hydrogen chloride/ether solution at room temperature. The precipitate which has separated out is filtered off with suction, rinsed with a little ether and dried at 40° C. in vacuo. 6.5 g (89% of theory, based on the base employed) of 3-(4-chlorophenoxy)-2-(4-chlorophenyl)-3-methyl-1-(1,2,4-triazol-1-yl)-2-butanol hydrochloride of melting point 135° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04584308 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-6d471bfbc86a4721be5119673c58764a |
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| Source note | uspto-grants-1986_04 |
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