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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402581Generated: November 2, 2026

Potassium thiocyanate → HCID 178427859, compound

https://huagongshe.com/reaction/402581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium thiocyanateHCID 516872—
Reactant5-(2-Cyclopropyl-2-oxoethylamino)-2-fluoro-4-methylbenzonitrileHCID 86691247—
SolventAcetic AcidHCID 176—
ProductHCID 178427859HCID 17842785985.3%

Reaction Conditions

Temperature110 °C

Reaction Steps

5-(2-Cyclopropyl-2-oxoethylamino)-2-fluoro-4-methylbenzonitrile (14.19 g, 61.2 mmol) was dissolved in glacial acetic acid (300 mL). Potassium thiocyanate (11.9 g, 122.4 mmol) was added as a solid with stirring. The reaction mixture was heated to 110° C. for 4 hours at which time the solvent was removed under reduced pressure. The residue was taken up in dichloromethane (200 mL) and washed with 200 mL water. The aqueous extract was extracted with (2×200 mL) additional dichloromethane, the organic extracts combined and dried over magnesium sulfate. The solvent was removed under reduced pressure and the oily residue was re-dissolved in EA (50 mL) and 150 mL hexanes was added. A dark layer formed and a stir bar was added to the flask. Vigorous stirring caused the product to precipitate as a peach colored solid. The product was collected by filtration, to yield 5-(4-cyclopropyl-2-mercapto-1H-imidazol-1-yl)-2-fluoro-4-methylbenzonitrile, (14.26 g, 52.23 mmol). Anal. LC/MS (m/z: 274, M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742126B2
Source datasetuspto-grants-2014_06
ORD IDord-7283f7f15d20406c8bb9f586802ddc2f
Source noteuspto-grants-2014_06