HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613394Generated: October 29, 2026
1H-1,2,4-Triazole → HCID 15433416, compound
https://huagongshe.com/reaction/613394
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(2,4-Difluorophenyl)-1,1-difluoro-1-(2-methoxyethyl)thio-2,3-epoxypropane | HCID 15434383 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 15433416 | HCID 15433416 | 12.4% |
Reaction Steps
To a solution of 2-(2,4-difluorophenyl)-1,1-difluoro-1-[(2-methoxyethyl)thio]-2,3-epoxypropane (13.0 g, 0.044 mol) in DMSO (100 ml), 1,2,4-triazole (7.6 g, 0.11 mol) and potassium carbonate (15.2 g, 0.11 mol) were added and the resulting mixture was stirred at room temperature for 12 hours and at an external temperature of 50° C. for one hour. After the completion of the reaction, the reaction mixture was diluted with ether and insoluble matter was filtered off. The ether solution was washed with water, dried over magnesium sulfate and distilled off under reduced pressure. The residue was recrystallized from isopropyl ether-ethyl acetate, whereby 2-(2,4-difluorophenyl)-1,1-difluoro-1-[(2-methoxyethyl)thio]-3-(1H-1,2,4-triazol-1-yl)-2-propanol (2.0 g, yield: 12.0%) was obtained as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06008239 |
|---|
| Source dataset | uspto-grants-1999_12 |
|---|
| ORD ID | ord-15fd9a3188044b8b8f147b93b4373b2a |
|---|
| Source note | uspto-grants-1999_12 |
|---|