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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509649Generated: October 31, 2026

Potassium Carbonate → HCID 114798686, compound

https://huagongshe.com/reaction/1509649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,2-Diaminocyclohexane, trans-HCID 43806—
ReactantBenzene, 1-iodo-3-methoxy-HCID 69839—
Reactant4-PhenylpyrazoleHCID 139106—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 114798686HCID 114798686—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 4-phenyl-1H-pyrazole (775 mg, 5.38 mmol, 1.0 eq), 1-iodo-3-methoxybenzene (1510 mg, 768 μL, 6.45 mmol, 1.2 eq), CuI (21 mg, 0.11 mmol, 0.02 eq), K2CO3 (1561 mg, 11.30 mmol, 2.1 eq) and trans-1,2-cyclohexanediamine (123 mg, 1.08 mmol, 0.20 eq) in dioxane (12 mL) was stirred at a temperature of 110° C. for three days, then cooled to ambient temperature. The solvent was removed under reduced pressure and the residue was purified through column chromatography on silica gel using hexane and ethyl acetate (10:1-5:1-3:1) as an eluent to obtain the desired product, 1-(3-methoxyphenyl)-4-phenyl-1H-pyrazole 5, as a colorless liquid (1.13 g in 84% yield). 1H NMR (DMSO-d6, 400 MHz): δ 3.84 (s, 3H), 6.87-6.90 (m, 1H), 7.25 (t, J=7.2 Hz, 1H), 7.38-7.48 (m, 5H), 7.71 (d, J=7.2 Hz, 2H), 8.20 (s, 1H), 9.01 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09224963B2
Source datasetuspto-grants-2015_12
ORD IDord-ac02d1f5f07241b7b8717a6660b69a20
Source noteuspto-grants-2015_12