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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292876Generated: October 30, 2026

Potassium Iodide → HCID 15279827, compound

https://huagongshe.com/reaction/2292876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2,3-DichloropropeneHCID 6565—
ReactantPotassium CarbonateHCID 11430—
Reactant(3,5-Dichlorophenyl)cyanamideHCID 23279465—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 15279827HCID 1527982790%

Reaction Conditions

Temperature50 °C

Reaction Steps

N-(3,5-dichlorophenyl)cyanamide (2.81 g) was dissolved in DMF (14.03 g), to which powdered potassium carbonate (3.11 g) and potassium iodide (0.26 g) were added at room temperature with stirring. Further, 2,3-dichloro-1-propene (2.00 g) was added dropwise at room temperature with stirring. The mixture was heated to 50° C. and stirred at the same temperature for 2.5 hours. After cooling to room temperature, DMF (9.00 g) and ammonium sulfide solution, yellow (8.00 g) having an S content of 6% were added dropwise to the reaction mixture at room temperature with stirring. The mixture was heated to 50° C. and stirred at the same temperature for 4 hour. After cooling to room temperature, water 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 4.00 g of N-(3,5-dichlorophenyl)-N-(2-chloro-2-propenyl)thiourea as a dark red solid (90% yield in appearance). The percentage area of liquid chromatography was 94%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05684196
Source datasetuspto-grants-1997_11
ORD IDord-28b00fa711b54d628d572762d71db88c
Source noteuspto-grants-1997_11