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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276420Generated: November 3, 2026

Potassium Cyanide → 2-(1-Chloro-cyclopropyl)-1-(2-chloro-phenyl)-3-(5-thiocyanato-1,2,4-triazol-1-yl)-propan-2-ol

https://huagongshe.com/reaction/1276420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantChlorineHCID 24526—
ReactantHCID 178520209HCID 178520209—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product2-(1-Chloro-cyclopropyl)-1-(2-chloro-phenyl)-3-(5-thiocyanato-1,2,4-triazol-1-yl)-propan-2-olHCID 1087231165%

Reaction Conditions

Temperature20 °C

Reaction Steps

At 20° C., chlorine gas is introduced into a mixture of 1.72 g (5 mmol) of 2-(1-chloro-cyclopropyl)-1-(2-chloro-phenyl)-3-(5-mercapto-1,2,4-triazol-1-yl)-propan-2-ol and 0.65 g (10 mmol) of potassium cyanide in 20 ml of acetic acid. The reaction mixture is stirred at 20° C. for 20 hours and then diluted with dichloromethane. The mixture is then extracted repeatedly with dilute aqueous sodium hydroxide solution and the organic phase is dried over sodium sulphate and concentrated under reduced pressure. The product that remains is purified over silica gel using petroleum ether/ethyl acetate=1:1 as mobile phase. Concentration of the eluate gives 1.2 g (64% of theory) of 2-(1-chloro-cyclopropyl)-1-(2-chloro-phenyl)-3-(5-thiocyanato-1,2,4-triazol-1-yl)-propan-2-ol in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166059
Source datasetuspto-grants-2000_12
ORD IDord-a268c1ea0396449d817701adae346bd2
Source noteuspto-grants-2000_12