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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742117Generated: November 3, 2026

1H-1,2,4-Triazole → HCID 10946371, compound

https://huagongshe.com/reaction/1742117

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
Reactant4-Chloro-α-(chloromethyl)-α-(1-fluorocyclopropyl)benzeneethanolHCID 11097380—
SolventDimethylformamideHCID 6228—
ProductHCID 10946371HCID 1094637135%

Reaction Conditions

Temperature80 °C

Reaction Steps

Under an atmosphere of nitrogen, 27.6 g (0.4 mol) of 1,2,4-triazole and 33.6 g (0.3 mol) of potassium tert.-butylate in 100 ml of absolute dimethylformamide are introduced as an initial charge and heated to 80° C. At this temperature, a solution of 26.3 g (0.1 mol) of 1-chloro-2-(1-fluoro-cyclopropyl)-3-(4-chlorophenyl)-propan-2-ol in 50 ml of absolute dimethylformamide is added dropwise thereto while stirring. The mixture is stirred for another 6 hours at 100° C. and then concentrated by stripping off the diluent under reduced pressure. The residue is taken up in ethyl acetate, the solution is washed with water, and, after drying over sodium sulphate, the solvent is evaporated under reduced pressure. The product left behind is chromatographed on a silica gel column, using chloroform as the mobile solvent. In this way, 8.9 g (35% of theory) of 1-(4-chlorophenyl)-2-(1-fluoro-cyclopropyl)-3-(1,2,4-triazol-1-yl)-propan-2-ol are obtained in the form of a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05336809
Source datasetuspto-grants-1994_08
ORD IDord-4ba2c8fc4e584fbaa41b104b8df6b260
Source noteuspto-grants-1994_08