The important role of 484-47-9

Although many compounds look similar to this compound(484-47-9)Category: nitriles-buliding-blocks, numerous studies have shown that this compound(SMILES:C1(C2=CC=CC=C2)=NC(C3=CC=CC=C3)=C(C4=CC=CC=C4)N1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 2,4,5-Triphenylimidazole( cas:484-47-9 ) is researched.Category: nitriles-buliding-blocks.Gabla, Jenifer J.; Lathiya, Dharmesh R.; Revawala, Akash A.; Maheria, Kalpana C. published the article 《Propyl-SO3H functionalized SBA-15: Microwave-mediated green synthesis of biologically active multi-substituted imidazole scaffolds》 about this compound( cas:484-47-9 ) in Research on Chemical Intermediates. Keywords: SBA15 propysulfate catalyst preparation multicomponent heterocyclization catalyst; imidazole multicomponent solventless green synthesis; microwave irradiation multicomponent solventless heterocyclization mediator. Let’s learn more about this compound (cas:484-47-9).

Propylsulfonic acid functionalized Santa Barbara Amorphous-15 (SBA-15-Pr-SO3H) catalyst has been synthesized using a surface modification of mesoporous SBA-15 via the one-pot co-condensation method. The synthesized SBA-15-Pr-SO3H has been characterized by peculiar characterization techniques such as small- and wide-angle XRD, SEM-EDX, TEM, TG-DTA, acidity, FT-IR, Py-FT-IR and BET surface area anal. The catalytic activity of synthesized catalyst has been studied towards solvent-free MW irradiation for the green and rapid synthesis of multi-substituted imidazoles, [2,4,5-triphenyl-1(H)-imidazole (tri-imidazole) and 1-benzyl-2,4,5-triphenyl-1H-imidazole (tetra-imidazole)]. The SBA-15-Pr-SO3H catalyst was found to be an efficient and recyclable solid acid catalyst and this solvent-free MW protocol afforded products in good to excellent yields of both, tri and tetra imidazoles (> 95%) within shorter reaction time (3 min) at 600 W as compared to the SBA-15 and other existing protocols. The applicability of this protocol was further explored by conducting the experiments in the presence of varied solvents and substituted aldehydes to generate a library of both, tri- and tetra-imidazole scaffolds. The catalyst was found to be reusable up to several runs without loss of its catalytic activity. This report allows the rapid and scalable access to a variety of multi-substituted imidazoles using SBA-15-Pr-SO3H, as heterogeneous catalyst.

Although many compounds look similar to this compound(484-47-9)Category: nitriles-buliding-blocks, numerous studies have shown that this compound(SMILES:C1(C2=CC=CC=C2)=NC(C3=CC=CC=C3)=C(C4=CC=CC=C4)N1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts