HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371912Generated: October 27, 2026
Potassium Carbonate → 1-(4-Chlorobenzoyl)-1-(3-chloro-1,2,4-triazol-1-yl)-cyclopropane
https://huagongshe.com/reaction/2371912
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-4-chloro-1-(4-chlorophenyl)butan-1-one | HCID 107167 | — |
| Reactant | HCID 178478410 | HCID 178478410 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(4-Chlorobenzoyl)-1-(3-chloro-1,2,4-triazol-1-yl)-cyclopropane | HCID 14697227 | 90% |
Reaction Steps
A mixture of 34 g (246 mmol) of potassium carbonate and 35 g (338 mmol) of 3-chloro-1,2,4-triazole in 130 ml of acetone is refluxed. To this mixture there is added dropwise a solution of 50 g (169 mmol) of 2-bromo-4-chloro-1-(4-chlorophenyl)-butan-1-one in 60 ml of acetone. The mixture is boiled under reflux for a further 8 hours, the solid residue is then filtered off with suction, and the solvent is stripped off under reduced pressure. The residue which remains is taken up in ethyl acetate. The solution is washed with water, dried over sodium sulphate and concentrated under reduced pressure. The residue which remains is chromatographed on silica gel using dichloromethane as the eluent. Concentration of the eluate by evaporation gives 42.9 g (90% of theory) of 1-(4-chlorobenzoyl)-1-(3-chloro-1,2,4-triazol-1-yl)-cyclopropane in the form of a solid of melting point 85° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05096913 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-f0e212b1dd4042c7b53846df5a505cd3 |
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| Source note | uspto-grants-1992_03 |
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