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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951465Generated: November 3, 2026

Potassium Iodide → HCID 178521931, compound

https://huagongshe.com/reaction/1951465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 178508055HCID 178508055—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventAcetoneHCID 180—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 178521931HCID 17852193121.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

An aqueous solution of sodium nitrite (760 mg) in 2 ml of water was added drop wise to a stirred suspension of 4-amino-1H-pyrazole-3-carboxylic acid phenylamide (2 g; 10 mmol) in concentrated hydrochloric acid (20 ml) at 0° C., then stirred at 0° C. for a further 60 minutes. The reaction mixture was diluted with acetone (10 ml) then treated with potassium iodide (1.8 g) and copper (I) iodide (2.1 g) and stirred at room temperature for 90 minutes. The reaction mixture was diluted with brine and ethyl acetate then washed with saturated sodium thiosulphate solution. The ethyl acetate layer was separated, dried (MgSO4), filtered and evaporated to give 680 mg of 4-iodo-1H-pyrazole-3-carboxylic acid phenylamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404718B2
Source datasetuspto-grants-2013_03
ORD IDord-ac58ab1351a9450eb0b940a0889fde35
Source noteuspto-grants-2013_03