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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004665Generated: October 30, 2026

4-Chlorobenzoyl chloride → 2-(1-Chloro-cyclopropyl)-1-(2-chlorophenyl)-3-[5-(4-chloro-benzoyl-mercapto)-1,2,4-triazol-1-yl]-propan-2-ol

https://huagongshe.com/reaction/1004665

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178520209HCID 178520209—
SolventTetrahydrofuranHCID 8028—
Product2-(1-Chloro-cyclopropyl)-1-(2-chlorophenyl)-3-[5-(4-chloro-benzoyl-mercapto)-1,2,4-triazol-1-yl]-propan-2-olHCID 1790995599.4%

Reaction Steps

At room temperature, a solution of 0.63 ml (5 mmol) of 4-chloro-benzoyl chloride in 5 ml of absolute tetrahydrofuran is added dropwise with stirring to a mixture of 1.72 g (5 mmol) of 2-(1-chloro-cyclopropyl)-1-(2-chlorophenyl)-3-(5-mercapto-1,2,4-triazol-1-yl)-propan-2-ol, 0.69 g (5 mmol) of anhydrous potassium carbonate and 20 ml of absolute tetrahydrofuran. The reaction mixture is stirred at room temperature for a further 20 hours and then filtered off with suction and concentrated under reduced pressure. In this manner, 2.4 g (99% of theory) of 2-(1-chloro-cyclopropyl)-1(2-chlorophenyl)-3-[5-(4-chloro-benzoyl-mercapto)-1,2,4-triazol-1-yl]-propan-2-ol are obtained in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051592
Source datasetuspto-grants-2000_04
ORD IDord-61a411898c2c4502b50eb8ef1358da6b
Source noteuspto-grants-2000_04