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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238371Generated: October 30, 2026

Potassium Carbonate → 2-Methyl-1'-[4-(trifluoromethyl)phenyl]-1'H,2H-3,4'-bipyrazole

https://huagongshe.com/reaction/238371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
ReactantBenzene, 1-iodo-4-(trifluoromethyl)-HCID 67993—
Reactanttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
Reactant2-Methyl-1'H,2H-3,4'-bipyrazoleHCID 136387776—
CatalystCopper iodideHCID 83717—
SolventDimethylformamideHCID 6228—
Product2-Methyl-1'-[4-(trifluoromethyl)phenyl]-1'H,2H-3,4'-bipyrazoleHCID 8955874080.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

Under a nitrogen atmosphere, a mixture of 2-methyl-1′H,2H-3,4′-bipyrazole (176 mg), 4-iodobenzotrifluoride (485 mg), copper iodide (45 mg), potassium carbonate (329 mg), trans-N,N′-dimethylcyclohexan-1,2-diamine (135 mg) and N,N-dimethylformamide (2.2 mL) was stirred at 100° C. for 16 hours. Thereafter, a saturated ammonium chloride aqueous solution was added to the reaction solution, and the obtained mixture was then extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate, and was then concentrated under a reduced pressure. The residue was purified by column chromatography (silica gel cartridge, hexane:ethyl acetate=9:1 to 1:1), so as to obtain the title compound (280 mg) in the form of a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642626B2
Source datasetuspto-grants-2014_02
ORD IDord-325bb98fb8fd415ea261e8d718bd0fed
Source noteuspto-grants-2014_02