HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477401Generated: October 29, 2026
1H-1,2,4-Triazole → HCID 14330161, compound
https://huagongshe.com/reaction/477401
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | HCID 14330160 | HCID 14330160 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14330161 | HCID 14330161 | 72% |
Reaction Steps
37 g (0.138 mol) of 2-(4-chlorophenyl)-2-(tetrahydro-2H-pyran-2-yl-oxymethyl)-oxirane are added to a mixture of 22.4 g (0.32 mol) of 1,2,4-triazole, 5 g (0.04 mol) of potassium tert.-butylate and 300 ml of dimethylformamide at room temperature, while stirring. After the addition has ended, the reaction mixture is stirred at 80° C. for 12 hours and is then concentrated by stripping off the solvent under reduced pressure. Water is added to the residue which remains, the resulting mixture is extracted three times with methylene chloride and the combined organic phases are dried over magnesium sulphate and concentrated by stripping off the solvent under reduced pressure. The product thus obtained is purified chromatographically on silica gel with methylene chloride/ethyl acetate =4:1 as the mobile phase. 33.5 g (72% of theory) of 2-(4-chlorophenyl)-1-[(tetrahydro-2H-pyran-2-yl)-oxy]-3-(1,2,4-triazol-1-yl)-propan-2-ol are obtained in this manner in the form of pale yellow crystals of melting point 70° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04888048 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-d0938c004afb499db80e28149e1b4986 |
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| Source note | uspto-grants-1989_12 |
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