首页> 外文期刊>Indian Journal of Chemistry, Section B. Organic Including Medicinal >A mild and efficient synthesis of bis(indolyl)methane derivatives catalyzed by monoammonium salt of 12-tungstophosphoric acid
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A mild and efficient synthesis of bis(indolyl)methane derivatives catalyzed by monoammonium salt of 12-tungstophosphoric acid

机译:12-钨磷酸一铵盐催化温和高效地合成双(吲哚基)甲烷衍生物

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摘要

A simple, highly rapid and efficient electophilic substitution reaction of indole with various aromatic aldehydes has been carried out using 5 wt% of monoammonium salt of 12-tungstophosphoric acid [(NH4)OH2PW_(12)O_(40)] as a solid acid catalyst in acetonitrile to afford the corresponding bis(indolyl)methanes in excellent yields (84-95%) at room temperature. The heteropolyacid-based catalyst has the advantages of simple workup procedure, water insolubility with good activity and high yielding reaction for the synthesis of bis(indolyl)methane derivatives.
机译:使用5 wt%的12-钨磷酸单铵盐[(NH4)OH2PW_(12)O_(40)]作为固体酸催化剂,进行了吲哚与各种芳族醛的简单,快速,高效的亲电子取代反应在室温下,用乙腈洗脱得到相应的双(吲哚基)甲烷,收率极高(84-95%)。该杂多酸基催化剂的优点是后处理步骤简单,水不溶性好,活性好,合成双(吲哚基)甲烷衍生物的产率高。

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