HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345862Generated: October 29, 2026
1H-1,2,4-Triazole → HCID 14798970, compound
https://huagongshe.com/reaction/345862
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | HCID 14798951 | HCID 14798951 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 14798970 | HCID 14798970 | — |
Reaction Steps
2.42 g (11 mmol) of trimethylsulphoxonium iodide (EGA) are added in portions at 20° C. to a suspension of 0.33 g (11 mmol) of sodium hydride (80% in oil) in 20 ml of DMSO p.a. The mixture is stirred until evolution of hydrogen has ended and 2 g (10mmol) of (4-fluoro)-1-benzoyl-1-cyanocyclopropane, dissolved in 5 ml of abs. DMSO, are rapidly added dropwise. The mixture is stirred for 1 h at RT and for 1 h at 40° C., then 1.04 g (15 mmol) of 1,2,4-triazole (sublimed) and 0.46 g (5 mmol) of 1,2,4-triazole Na salt in DMSO are added. The mixture is stirred for 2 h at 50° C. and for 4 h at 80° C., poured into ice-water and extracted using dichloromethane. The organic phase is washed with 2N sodium hydroxide solution, dried over Na2SO4 and concentrated. The residue is chromatographed on silica gel and the product is crystallized from diethyl ether. 1.2 g (44% of theory) of colorless crystals of 1-(1-cyanocyclopropyl)-1-(4-fluorophenyl)-2-(1,2,4-triazol-1-yl)ethanol are thus obtained having a melting point of 121°-122° C.,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05059615 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-7ee8b58ee5f74a96ad37b8f57f969be3 |
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| Source note | uspto-grants-1991_10 |
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