(3,5-Di-<i>tert</i>-butylphenyl)(1<i>H</i>-pyrazol-1-yl)methanone

Abstract

The acyl pyrazole derivative (3,5-di-tert-butylphenyl)(1H-pyrazol-1-yl)methanone was prepared simply and rapidly in 86% isolated yield by means of an oxidative functionalization reaction of an aldehyde with pyrazole. A substoichiometric quantity of 4-acetamido-2,2,6,6-tetramethylpiperidine-1-oxoammonium nitrate was used as the oxidant. The reaction was performed solvent-free and in the absence of a base, making it a clean, green approach. The mixture of aldehyde, pyrazole, and the oxidant was heated at 55 °C for 3 h, and then, the product was isolated in analytically pure form via extraction with no need for column chromatography.

Keywords

• oxoammonium salt
• oxidative functionalization
• aldehyde
• pyrazole
• acyl pyrazole
• green chemistry