Lasri Condensation

The Lasri condensation^{[non-primary source needed]} is an organic chemistry reaction where chalcone reacts with a hydrazone to furnish an azine and 3,5-diphenyl-1H-pyrazole.^[1] It is named after the Portuguese-Moroccan chemist Jamal Lasri.^{[2][non-primary source needed]}

Mechanism

The reaction is started with nucleophilic attack of the amino moiety of hydrazone 1 on the carbonyl group of (E)-1,3-diphenyl-2-propenone 3 to produce the azine intermediate 1-((E)-1,3-diphenylallylidene)-2-(diarylmethylene)hydrazine. This asymmetrical azine then undergoes nucleophilic attack from its diaryl imino sp²-carbon atom by the amino NH₂ moiety of hydrazone 1 to afford a second intermediate where the C(sp³)—N bond is cleaved to furnish the symmetrical azine 2. The other product, 1,3-diphenyl-2-propenone hydrazone 3a, cyclizes to afford 2,3-dihydro-3,5-diphenyl-1H-pyrazole^[3] which is then rapidly dehydrogenated to yield 3,5-diphenyl-1H-pyrazole 4.^[4] In this reaction hydrazone 1 is a source of nitrogen for 3,5-diphenyl-1H-pyrazole 4. Additionally, the reaction does not require the use of any catalyst or promoter.

References

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