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首页> 外文期刊>Monatshefte fur Chemie >Solvent-free synthesis of amidoalkyl naphthols in the presence of MWCNTs@SiO2/SO3H as effective solid acid catalyst
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Solvent-free synthesis of amidoalkyl naphthols in the presence of MWCNTs@SiO2/SO3H as effective solid acid catalyst

机译:在MWCNTS / SIO2 / SO3H存在下,无溶剂合成氨基烷基萘酚作为有效的固体酸催化剂

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摘要

Multiwalled carbon nanotubes (MWCNTs) were modified with sulfonic acid groups through a new method. In the first step, MWCNTs' surfaces were hydroxylated using KMNO4 as oxidating agent and a surfactant (TPABr). Second, SiO2-coated MWCNTs were prepared through the reaction of hydroxylated CNTs with tetraethyl orthosilicate, and in last step, MWCNTs@SiO2/SO3H was prepared using the reaction of MWCNTs@SiO2 with ClSO3H. Obtained catalyst was used as efficient solid acid catalyst for one-pot three-component condensation reaction of 2-naphthol, benzaldehyde, and amide derivatives to afford the corresponding amidoalkyl naphthols. The reaction was performed under solvent-free conditions and products were obtained in high to excellent yields (80-98%). Prepared solid acid catalyst was characterized using FT-IR, BET, TGA, SEM, and EDX techniques. Presented methodology has several advantages such as simple procedure, excellent yields of products, effective reusable solid acid catalyst, and eco-friendly reaction conditions.
机译:通过新方法用磺酸基改性多壁碳纳米管(MWCNT)。在第一步中,使用KMNO4作为氧化剂和表面活性剂(TPABR),将MWCNTS表面羟基化。第二,通过将羟基化的CNT与四乙基硅酸盐的反应反应制备SiO 2涂覆的MWCNT,并且在最后一步中,使用MWCNTS / SiO 2与CLSO3H的反应制备MWCNTS @ SiO 2 / SO 3H。将获得的催化剂用作2-萘酚,苯甲醛和酰胺衍生物的一锅三元组分缩合反应的有效固体酸催化剂,得到相应的丙二烷基萘酚。反应在无溶剂条件下进行,并以高于优异的产率(80-98%)获得产物。使用FT-IR,BET,TGA,SEM和EDX技术表征制备的固体酸催化剂。呈现的方法具有若干优点,如简单的程序,优异的产品产量,有效可再使用的固体酸催化剂和环保反应条件。

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