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首页> 外文期刊>Reactive & Functional Polymers >Highly selective tetrahydropyranylation/dehydropyranylation of alcohols and phenols using porous phenolsulfonic acid-formaldehyde resin catalyst under solvent-free condition
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Highly selective tetrahydropyranylation/dehydropyranylation of alcohols and phenols using porous phenolsulfonic acid-formaldehyde resin catalyst under solvent-free condition

机译:在无溶剂条件下使用多孔酚磺酸-甲醛树脂催化剂对醇和酚进行高选择性四氢吡喃基化/脱氢吡喃基化

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摘要

An efficient protocol for solvent-free chemoselective tetrahydropyranylation/depyranylation of alcohols and phenols is reported herein using mesoporous Phenolsulfonic Acid Formaldehyde Resins as a heterogeneous acid catalyst. The catalyst successfully performed chemoselective protection and deprotection reactions of a wide range of substrates ranging from primary to secondary and tertiary alcohols and also phenols. The reactions were carried out at ambient temperature under solvent-free condition (SolFC) which resulted in high yields within a very short time. FT-IR, TEM, SEM, EDS and TG-DSC analysis techniques were employed to characterize the synthesized polymeric catalyst. The chemoselective nature of our method was confirmed using C-13 DEPT-135 NMR studies. The polymer catalyst was found to be recoverable even after 10th catalytic cycle without much depreciation in its activity. The heterogeneity of the catalyst was verified by hot filtration method. Good yield, energy and cost- effective method, solvent-free protocol, mild reaction conditions, no inert atmosphere, metal-free heterogeneous polymer catalyst and excellent recoverability of the catalyst are notable milestones of the reported protocol.
机译:本文报道了使用介孔酚磺酸甲醛树脂作为非均相酸催化剂的无溶剂的醇和酚化学选择性四氢吡喃基化/脱吡喃基化的有效方案。该催化剂成功地进行了从伯醇到仲醇和叔醇以及酚类的多种底物的化学选择性保护和脱保护反应。反应在室温下在无溶剂条件下进行(SolFC),这导致在非常短的时间内获得高收率。 FT-IR,TEM,SEM,EDS和TG-DSC分析技术被用来表征合成的聚合物催化剂。使用C-13 DEPT-135 NMR研究证实了我们方法的化学选择性。发现该聚合物催化剂即使在第十次催化循环后仍可回收,而其活性没有很大的下降。通过热过滤法验证了催化剂的非均质性。良好的收率,能源和成本效益的方法,无溶剂方案,温和的反应条件,无惰性气氛,无金属的多相聚合物催化剂以及优异的催化剂可回收性是所报告方案的重要里程碑。

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