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New methodology for the preparation of 3-hydroxy-2-pyridinone (32-HOPO) chelators and extractants. Part 2. Reactions of alcohols phenols and thiols with an electrophilic 32-HOPO reagent

机译:制备3-羟基-2-吡啶酮(32-HOPO)螯合剂和萃取剂的新方法。第2部分。醇酚和硫醇与32-HOPO亲电试剂的反应

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摘要

The reactions of the electrophilic iminium ester mesylate salt >1 with alcohols, phenols and thiols has been investigated. In the presence of base, thiols, phenols and thiophenol react with >1 to give the corresponding ether linked HOPO derivatives in good yields. However, the ring opening of salt >1 with alcohols could only be accomplished efficiently using a large excess of the alcohol in the presence of methanesulfonic acid at 80°C. The synthetic utility of HOPO precursor, >1, has been demonstrated by the synthesis of two polyHOPO chelators >7 and >9.
机译:研究了亲电子亚氨基磺酸甲磺酸酯> 1 与醇,酚和硫醇的反应。在碱的存在下,硫醇,酚和硫酚与> 1 反应,以高收率得到相应的醚键连接的HOPO衍生物。然而,盐> 1 与醇的开环只有在甲烷磺酸在80°C的条件下使用大量过量的醇才能有效地完成。 HOPO前体> 1 的合成效用已通过两种polyHOPO螯合剂> 7 和> 9 的合成得到证明。

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