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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650643Generated: October 28, 2026

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/650643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
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%

Reaction Steps

At room temperature, a solution of 0.63 ml (5 mmol) of 4-chloro-benzo)yl 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 numberUS06274610B1
Source datasetuspto-grants-2001_08
ORD IDord-9f81a0c10d9b46469d73763270dea143
Source noteuspto-grants-2001_08