cds nanoparticles: an efficient, clean and reusable heterogeneous catalyst for one-pot procedure for synthesis of 3,4-dihydropyrimidin-2(1h)-ones in solvent-free conditions
نویسندگان
چکیده
3,4-dihydropyrimidinones and their derivatives are synthesized via biginelli routes involving an aromatic aldehydes, ethylacetoacetates and urea in one-pot procedure by using cds nanoparticles as efficient heterogeneous catalyst in solvent-free conditions. compared with classical biginelli reaction reported in 1893, this new method provides much improved modification in terms of simplicity. the present methodology offers several advantages such as a simple procedure with an easy work-up, short reaction times and excellent yields. excellent yields and mild reaction conditions as well as the environmentally friendly character of cds make it an important alternative to the classic acid catalyzed biginelli's reactions. the catalysts could be recycled and reused for five times, without substantial reduction in their catalytic activities. the results are shown that electron-releasing group on aromatic ring causes reduced rate of reaction and electron with drawing group's causes increased the rate of reactions. the structure of products has been characterized by ir and 1hnmr spectra.
منابع مشابه
CdS nanoparticles: An efficient, clean and reusable heterogeneous catalyst for one-pot procedure for synthesis of 3,4-Dihydropyrimidin-2(1H)-ones in solvent-free conditions
3,4-Dihydropyrimidinones and their derivatives are synthesized via Biginelli routes involving an aromatic aldehydes, ethylacetoacetates and urea in one-pot procedure by using CdS nanoparticles as efficient heterogeneous catalyst in solvent-free conditions. Compared with classical Biginelli reaction reported in 1893, this new method provides much improved modification in terms of simplicity. The...
متن کاملCdS nanoparticles: An efficient, clean and reusable heterogeneous catalyst for one-pot procedure for synthesis of 3,4-Dihydropyrimidin-2(1H)-ones in solvent-free conditions
3,4-Dihydropyrimidinones and their derivatives are synthesized via Biginelli routes involving an aromatic aldehydes, ethylacetoacetates and urea in one-pot procedure by using CdS nanoparticles as efficient heterogeneous catalyst in solvent-free conditions. Compared with classical Biginelli reaction reported in 1893, this new method provides much improved modification in terms of simplicity. The...
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An efficient protocol for the synthesis of 3,4-dihydropyrimidin-2-(1H)-one/thione derivatives via multi-component coupling reaction of aromatic aldehydes, β-ketoester and urea or thiourea under solvent-free conditions using Silica Supported Barium Chloride as a catalyst is described. All prepared compounds with melting points, IR,1H NMR and 13C NMR were identified. High yields, mild conditi...
متن کاملNano-Silica phosphoric acid: an efficient catalyst for one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones (thiones) under solvent-free or sonication conditions
Two simple protocols for the synthesis of three-component condensation reaction of an aldehyde, β-ketoester and urea or thiourea to obtain the 3, 4-dihydropyrimidin-2(1H)-ones (thiones) using nano silica phosphoric acid are reported. Short reaction times, high yields, reusability of catalyst and easy workup are some advantages of these protocols.
متن کاملNano-Silica phosphoric acid: an efficient catalyst for one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones (thiones) under solvent-free or sonication conditions
Two simple protocols for the synthesis of three-component condensation reaction of an aldehyde, β-ketoester and urea or thiourea to obtain the 3, 4-dihydropyrimidin-2(1H)-ones (thiones) using nano silica phosphoric acid are reported. Short reaction times, high yields, reusability of catalyst and easy workup are some advantages of these protocols.
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عنوان ژورنال:
international journal of bio-inorganic hybrid nanomaterialsجلد ۴، شماره ۴، صفحات ۲۲۵-۲۳۱
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