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三氟甲磺酸催化的少用量条件下的柱[n]芳烃的一锅法合成及溶液相反应机理研究。

One-pot synthesis of pillar[n]arenes catalyzed by a minimum amount of TfOH and a solution-phase mechanistic study.

机构信息

State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, China.

出版信息

Org Biomol Chem. 2012 Dec 21;10(47):9405-9. doi: 10.1039/c2ob26635k. Epub 2012 Oct 30.

Abstract

A practical and effective trifluoromethanesulfonic acid (TfOH)-catalyzed cyclooligomerization strategy was developed for the synthesis of functionalized pillar[n]arenes and copillar[5]arenes from 1,4-dialkoxybenzenes with paraformaldehyde under mild reaction conditions, and the reaction mechanism of solution-phase catalytic synthesis of pillararenes was investigated by room-temperature X-band ESR spectroscopy, mass spectroscopy, NMR and control experiments, suggesting a free radical process initially and a Friedel-Crafts alkylation process during the consequent coupling and ring-closure stage.

摘要

一种实用且有效的三氟甲磺酸(TfOH)催化环齐聚策略被开发出来,用于在温和的反应条件下,从对二甲氧基苯和多聚甲醛合成功能化的柱[n]芳烃和共柱[5]芳烃,通过室温 X 波段 ESR 光谱、质谱、NMR 和对照实验研究了柱芳烃溶液相催化合成的反应机理,表明自由基过程首先发生,随后在偶联和环化阶段发生傅-克烷基化反应。

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