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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352125Generated: November 2, 2026

1H-1,2,4-Triazole → 1-(4-Chlorobenzoyl)-1-(1,2,4-triazol-1-yl)cyclopropane

https://huagongshe.com/reaction/2352125

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-4-chloro-1-(4-chlorophenyl)butan-1-oneHCID 107167—
SolventAcetoneHCID 180—
Product1-(4-Chlorobenzoyl)-1-(1,2,4-triazol-1-yl)cyclopropaneHCID 1365045182.9%

Reaction Steps

A solution of 150 g of 4-chlorophenyl 1-bromo-3-chloropropyl ketone in 200 ml of acetone is added drop-wise to a boiling solution of 100 g of potassium carbonate and 110 g of 1,2,4-triazol in 400 ml of acetone, and the mixture is then stirred under reflux for 8 hours. Thereafter, it is evaporated down in vacuo, and the residue is stirred in 500 ml of water. The precipitate which separates out is filtered off under suction, washed several times with water and dried. 104 g (82% of theory) of 1-(4-chlorobenzoyl)-1-(1,2,4-triazol-1-yl)-cyclopropane of melting point 78° C. are obtained. ##STR56##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04875928
Source datasetuspto-grants-1989_10
ORD IDord-6f0cb39b6c9b465ea1a18d8209feabcb
Source noteuspto-grants-1989_10