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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650733Generated: November 1, 2026

1H-1,2,4-Triazole → HCID 14403430, compound

https://huagongshe.com/reaction/1650733

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2-(2,4-Dichlorophenylethenyl)-2-(1-propylmercaptocyclopropyl) oxiraneHCID 54087481—
SolventDimethylformamideHCID 6228—
ProductHCID 14403430HCID 1440343026%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 38.2 g (0.12 mol) of 2-(2,4-dichlorophenylethenyl)-2-(1-propylmercaptocyclopropyl) oxirane in 30 ml of dimethylformamide is added dropwise under a nitrogen atmosphere and with stirring at 80° C. to a mixture of 24 g (0.35 mol) of 1,2,4-triazole, 2.7 g (0.02 mol) of potassium tert.-butoxide and 50 ml of dimethylformamide. The mixture is stirred at 80° C. for 6 hours, then the solvent is removed under reduced pressure, and the residue is taken up in ethyl acetate/toluene, washed with water, dried over sodium sulphate and concentrated under reduced pressure. The residue which remains is chromatographed on silica gel using chloroform as the eluant. In this manner, 12.1 g (26% of theory) of trans-4-(2,4-dichlorophenyl)-2-(1-propylmercaptocyclopropyl)1-(1,2,4-triazol-1-yl)-but-3-en-2-ol are obtained in the form of an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925865
Source datasetuspto-grants-1990_05
ORD IDord-ba115882bbec43588ffe3edd859fcbaa
Source noteuspto-grants-1990_05