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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantSodium hydrideHCID 24758—
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
ReactantHCID 14798951HCID 14798951—
ReactantHCID 178418361HCID 178418361—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 14798970HCID 14798970—

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05059615
Source datasetuspto-grants-1991_10
ORD IDord-7ee8b58ee5f74a96ad37b8f57f969be3
Source noteuspto-grants-1991_10