Yoto Yusuke, Hatagochi Ryo, Irie Yuto, Takenaga Naoko, Kumar Ravi, Dohi Toshifumi
College of Pharmaceutical Sciences, Ritsumeikan University, 1-1-1 Nojihigashi, Kusatsu, Shiga, 525-8577, Japan.
Faculty of Pharmacy, Meijo University, 150 Yagotoyama, Tempaku-ku, Nagoya, 468-8503, Aichi, Japan.
Curr Org Synth. 2025;22(4):531-538. doi: 10.2174/0115701794298369240607042545.
An efficient method for synthesizing cyclic arylsulfonium salts has been developed by selective aryl transfer to the sulfur atom from aryl(mesityl)iodonium triflates, a recyclable series of diaryliodonium salts.
The utilization of sulfonium salts as valuable intermediates is well-established, as they exhibit high reactivity under conditions of heating or UV irradiation. However, their synthesis typically involves the reaction of diarysulfoxide with acid anhydride, which requires the oxidation of sulfur(II) to sulfoxide(IV) and thus limits the scope of synthesis. Hence, in this study, we employed recyclable mesityliodonium(III) salts and copper catalysis.
The method was used to synthesize cyclic arylsulfonium salts without the need for preoxidation of the sulfur atom, resulting in a facile and high-yield synthesis.
The desired cyclic arylsulfonium salts were synthesized through selective transfer of the aryl group from mesityliodonium salts, demonstrating the effectiveness of the new approach.
通过将芳基从芳基(均三甲苯基)三氟甲磺酸碘鎓盐(一种可循环使用的二芳基碘鎓盐系列)选择性转移至硫原子,已开发出一种合成环状芳基锍盐的有效方法。
锍盐作为有价值的中间体的应用已得到充分确立,因为它们在加热或紫外线照射条件下表现出高反应活性。然而,它们的合成通常涉及二芳基亚砜与酸酐的反应,这需要将硫(II)氧化为亚砜(IV),从而限制了合成范围。因此,在本研究中,我们采用了可循环使用的均三甲苯基碘鎓(III)盐和铜催化。
该方法用于合成环状芳基锍盐,无需对硫原子进行预氧化,从而实现了简便且高产率的合成。
通过均三甲苯基碘鎓盐的芳基选择性转移合成了所需的环状芳基锍盐,证明了新方法的有效性。