Deep eutectic solvent as a green catalyst for the one-pot multicomponent synthesis of 2-substituted benzothiazole derivatives.

The need for diverse essential chemicals and resources has markedly risen alongside the advancement of civilization. Regrettably, many toxic solvents used in chemical laboratories and industrial settings pose significant risks to the health of researchers and intensify environmental pollution. Deep eutectic solvents (DESs), serving as an alternative to ionic liquids, provide superior environmental benefits and have garnered significant interest in chemical research.

Boron-doped sulfonated graphitic carbon nitride as a highly efficient catalyst for the production of 5-hydroxymethylfurfural from carbohydrates.

The presence of humins during the conversion of concentrated fructose presents a major obstacle in the large-scale production of 5-hydroxymethylfurfural (HMF) from fructose. Herein, we reported a boron-doped graphitic carbon nitride sulfonated (BGCN-SOH) as an excellent catalyst for the synthesis of HMF from fructose. The BGCN-SOH catalyst structures were analyzed using various characterization techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), energy-dispersive X-ray spectroscopy (EDX), elemental mapping analysis, and Fourier-transform infrared spectroscopy (FT-IR).

One-Pot Effective Approach to 2,5-Diformylfuran From Carbohydrates Using MoS-Decorated Carbonaceous Sugarcane Bagasse.

Exploring the transformation of carbohydrates into valuable chemicals offers a promising and eco-friendly method for utilizing renewable biomass resources. Developing a bi-functional, sustainable heterogeneous catalyst is of utmost importance to attain a high level of selectivity for the desired product, 2,5-diformylfuran (DFF), in this direct conversion process. In this study, we developed a highly effective catalytic system to convert diverse carbohydrates into DFF.

Efficient conversion of carbohydrates into 5-hydroxymethylfurfural using choline chloride-based deep eutectic solvents.

In this study, the conversion of monosaccharides to 5-hydroxymethylfurfural (5-HMF) using different deep eutectic solvents (DESs) was investigated in various conditions. Among all the investigated DESs, [ChCl][trichloroacetic acid], based on choline chloride and trichloroacetic acid with the ratio 1:1, showed the highest catalytic activity. A maximum 5-HMF yield was 82 % for 1 h at 100 °C using [ChCl][trichloroacetic acid] as a catalyst from fructose.

Synthesis of benzo[]carbazole derivatives intramolecular cyclization using Brønsted acidic carbonaceous material as the catalyst.

In this work, a new procedure for the synthesis of benzo[]carbazole from 1,3-diketones, primary amines, phenylglyoxal monohydrate, and malononitrile employing a solid acidic catalyst has been developed. The multicomponent reaction provided 3-cyanoacetamide pyrrole as an intermediate and then the formation of benzo[]carbazole intramolecular ring closure. The reaction was carried out for 2 h at 240 °C, resulting in the desired product with 73% yield.

Conversion of cellulose into valuable chemicals using sulfonated amorphous carbon in 1-ethyl-3-methylimidazolium chloride.

In this study, three carbon-based solid acid catalysts were prepared the one-step hydrothermal procedure using glucose and Brønsted acid, including sulfuric acid, -toluenesulfonic acid, or hydrochloric acid. The as-synthesized catalysts were tested for their ability to convert cellulose into valuable chemicals. The effects of Brønsted acidic catalyst, catalyst loading, solvent, temperature, time, and reactor on the reaction were investigated.

A green approach for the synthesis of 2-substituted benzoxazoles and benzothiazoles coupling/cyclization reactions.

We have developed the green method for the synthesis of benzoxazoles and benzothiazoles with moderate to good yields using imidazolium chlorozincate (II) ionic liquid supported into FeO nanoparticles (LAIL@MNP) under solvent-free sonication. The reaction was performed under mild conditions and only produced water as a sole byproduct. The reactions under solvent-free sonication showed advantages of faster reaction rate (30 min) and high yields of the products (up to 90%).