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首页> 外文期刊>European journal of organic chemistry >P-(benzyloxy)calix[8]arene synthesis revisited: P-(benzyloxy)calix[4]-, p-(benzyloxy)calix[5]-, p-(benzyloxy)calix[7]-, and p-(benzyloxy)bis(homooxa) calix[4]arenes
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P-(benzyloxy)calix[8]arene synthesis revisited: P-(benzyloxy)calix[4]-, p-(benzyloxy)calix[5]-, p-(benzyloxy)calix[7]-, and p-(benzyloxy)bis(homooxa) calix[4]arenes

机译:对-(苄氧基)杯[8]芳烃合成进行了重新研究:对-(苄氧基)杯[4]-,对-(苄氧基)杯[5]-,对-(苄氧基)杯[7]-和对-(苄氧基)双(高氧)杯[4]芳烃

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摘要

A detailed investigation of the 4-(benzyloxy)phenol/formaldehyde reaction shows that along with the previously described p-(benzyloxy)calix[8]arene and p-(benzyloxy)calix[6]arene, others calixarenes are observed and easily recovered on a preparative scale. All these new calixarenes are opening interesting perspectives for the synthesis of new supramolecular hosts, easily functionalized at the para position under very mild conditions and/or exhibiting a deep hydrophobic pocket. During the course of the synthesis of p-(benzyloxy)calix[8]arene, compounds 4-7 are easily recovered as byproducts on a preparative scale. Alkylation of these new calixarenes leads to the first functionalized derivatives.
机译:对4-(苄氧基)苯酚/甲醛反应的详细研究表明,与先前描述的对-(苄氧基)杯[8]芳烃和对-(苄氧基)杯[6]芳烃一起,观察到其他cal芳烃并易于回收。在准备规模上。所有这些新的杯芳烃为合成新的超分子宿主打开了有趣的前景,这些宿主在非常温和的条件下易于在对位官能化和/或表现出深的疏水性。在对-(苄氧基)杯[8]芳烃的合成过程中,化合物4-7容易以制备规模作为副产物回收。这些新的杯芳烃的烷基化导致第一个功能化的衍生物。

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