Related Experiment Video
Updated: Jan 20, 2026

Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
Nano-NiCo2O4-catalyzed dehydrogenative direct esterification and amidation of primary alcohols under microwave
Kumari Anchal1, Keya Roy2, Laksmikanta Adak2
1Department of Chemistry, Guru Ghasidas Vishwavidyalaya Koni Bilaspur-495009 Chhattisgarh India ocsb2006@gmail.com.
Abstract:
Here, we demonstrate NiCo2O4 nanoparticle-catalyzed dehydrogenative esterification and amidation of primary alcohols to esters of fatty acids and amides under microwave irradiation, without the need for any oxidant, achieving excellent yields of esters (50-92%) and amides (72-80%). The NiCo2O4 nanomaterial was prepared through co-precipitation, and its composition, morphology, structure, and textural properties were analyzed via powder XRD, FESEM, EDX, TEM, and BET. The crystallite size was found to be 121.69 nm using the Scherrer equation, by considering the FWHM of the (311) diffraction plane. The FESEM and EDS analysis revealed the formation of spherical-shaped granules with a mean size of 0.251 µm and their elemental composition. Furthermore, HRTEM images with a mean size of 2.25 nm confirmed the formation of spherical NiCo2O4 nanoparticles. The mesoporous nature of the material is analyzed by the BET surface area (33.81 m2 g-1) and average pore diameter 23.49 nm. The NiCo2O4 nanoparticles remained stable throughout the reaction process and were reusable for up to eight cycles. The catalytic nature of NiCo2O4 has been proved by cyclic voltametric studies of fresh and recycled catalysts. The present dehydrogenative esterification and amidation protocol offers several advantages, for example, robust and recyclable NiCo2O4 nanoparticles as a catalyst, oxidant- and solvent-free reaction conditions, microwave-assisted faster reaction rate, excellent isolated yields of products, etc.
Related Concept Videos
12:07Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Esterification
The structure of an ester is a carbonyl with an alkyl or aryl group (R) on one side, and an oxygen bound to another alkyl or aryl group (R’) on the other side, represented by the general formula: RCOOR’. Esters can be commonly derived by an esterification reaction between a carboxylic acid and an alcohol. The hydroxyl group of the carboxylic acid is replaced by an alkyl or aryl group. Simple esters, which have low molecular weight and small R and R’ functional groups,...
Esterification
Esterification
07:57Effect of Microwave Synthesis Conditions on the Structure of Nickel Hydroxide Nanosheets
06:52Synthesis of Esters Via a Greener Steglich Esterification in Acetonitrile