Bhat, S.I.Choudhury, A.R.Trivedi, D.R.2026-02-052012RSC Advances, 2012, 2, 28, pp. 10556-10563https://doi.org/10.1039/c2ra21849fhttps://idr.nitk.ac.in/handle/123456789/26935The reaction of malononitrile with salicylaldehyde under solvent and catalyst free conditions was re-investigated using mechanochemical mixing, thermal heating and a direct crystallization process. The resulting condensation product by all three types of molecular activation, was found to be (2-amino-3-cyano-4H-chromene-4-yl)malononitrile, which is not the previously reported benzofuran-2-carbonitrile. The structure of the resulting chromene derivative was confirmed by FT-IR, MS, 1H, 13C NMR and single crystal and powder X-ray diffraction. The reaction pathway under neat conditions (mechanochemical mixing) at ambient temperature was monitored by IR spectral measurements. The versatility of the current green protocol was examined through the reaction of eleven derivatives of o-hydroxybenzaldehyde with malononitrile to obtain 2-amino-3-cyano-4H-chromene derivatives. In addition, malononitrile was further reacted with o-aminobenzaldehydes under neat conditions to yield quinoline derivatives. © 2012 The Royal Society of Chemistry.AldehydesMixingNuclear magnetic resonance spectroscopyX ray diffractionCatalyst-freeCatalyst-free synthesisChromene derivativesChromenesCondensation productCrystallization processMalononitrilesMechanochemicalsMolecular activationQuinoline derivativeReaction pathwaysSalicyl aldehydeSingle-crystal and powderSpectral measurementThermal heatingCatalysts