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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265733Generated: October 26, 2026

Potassium Iodide → N-(3-(trifluoromethyl)phenyl)-N-(2-chloro-2-propenyl)cyanamide

https://huagongshe.com/reaction/265733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2,3-DichloropropeneHCID 6565—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Trifluoromethyl)phenylcyanamideHCID 11074102—
SolventDimethylformamideHCID 6228—
ProductN-(3-(trifluoromethyl)phenyl)-N-(2-chloro-2-propenyl)cyanamideHCID 2148005599.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

N-(3-(trifluoromethyl)phenyl)cyanamide (18.6 g) was dissolved in N,N-dimethylformamide (DMF) (93.0 g), to which powdered potassium carbonate (20.7 g) and potassium iodide (1.7 g) were added at room temperature with stirring. Further, 2,3-dichloro-1-propene (13.3 g) was added dropwise at room temperature with stirring. The mixture was heated to 50° C. and stirred at the same temperature for 1 hour. After cooling to room temperature, waster was added to the reaction mixture, which was then extracted with ethyl acetate. The organic layer was washed with water. The solvent was removed by distillation under reduced pressure, which afforded 25.8 g of N-(3-(trifluoromethyl)phenyl)-N-(2-chloro-2-propenyl)cyanamide as an oil (99% yield in appearance). The percentage areas of gas chromatography and liquid chromatography were 98% and 99%, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05648533
Source datasetuspto-grants-1997_07
ORD IDord-68dee3052fa64740bd0a018fac86481b
Source noteuspto-grants-1997_07