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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512610Generated: October 27, 2026

Potassium Carbonate → 4-(1-(tris(4-methoxyphenyl)methyl)-1H-pyrazol-4-yl)benzaldehyde

https://huagongshe.com/reaction/512610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Formylphenylboronic AcidHCID 591073—
Reactant4-bromo-1-(tris(4-methoxyphenyl)methyl)-1H-pyrazoleHCID 58432066—
CatalystHCID 178418397HCID 178418397—
SolventWater 1,2-dimethoxyethaneHCID 18180031—
Product4-(1-(tris(4-methoxyphenyl)methyl)-1H-pyrazol-4-yl)benzaldehydeHCID 5843211783.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-bromo-1-(tris(4-methoxyphenyl)methyl)-1H-pyrazole (1.47 g, 3.1 mmol), (4-formylphenyl)boronic acid (0.94 g, 6.3 mmol), and K2CO3 (0.65 g, 4.7 mmol) in DME-H2O (25 mL, 4:1) was degassed by alternately putting under house vacuum and argon three times for several minutes each. Tetrakis(triphenylphosphine)palladium (0.35 g, 0.3 mmol) was added then the mixture was degassed again. After heating for 16.5 hrs at 80° C. and cooling to room temperature, H2O was added. The mixture was extracted with EtOAc and the combined organics were washed with H2O, saturated aqueous NaHCO3 and brine then dried over Na2SO4 and concentrated in vacuo. Purification by chromatography (20-30% EtOAc-hexanes; EtOAc containing 1% Et3N) gave 4-(1-(tris(4-methoxyphenyl)methyl)-1H-pyrazol-4-yl)benzaldehyde (1.31 g combined from two reactions, 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102643B2
Source datasetuspto-grants-2015_08
ORD IDord-12cfa1a912b94835abb78142c307708d
Source noteuspto-grants-2015_08