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Selective synthesis of α-organylthio esters and α-organylthio ketones from β-keto esters and sodium

机译:β-酮酯和钠的选择性合成α-氧化酮酯和α-氧化酮酮

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摘要

We described herein a selective method to prepare α-organylthio esters and α-organylthio ketones by the reaction of β-keto esters with sodium S-benzyl sulfurothioate or sodium S-alkyl sulfurothioate (Bunte salts) under basic conditions in toluene as the solvent at 100 °C. When 4 equivalents of a base were used, a series of differently substituted α-thio esters were obtained with up to 90% yield. On the other hand, employing 2 equivalents of a base, α-thio ketones were achieved after 18 h under air. Furthermore, after a shorter reaction time, the isolation of keto–enol tautomers was possible, revealing them as significant intermediates for the mechanism elucidation.
机译:我们在本文中描述了一种选择性方法,通过在甲苯的基本条件下,通过β-酮酯与S-苄基磺基噻嗪(Bunte Salts)的β-酮酯的反应制备α-氧化酯和α-氧化钠酸钠(Bunte Salts)作为溶剂100°C。当使用4当量的碱时,得到一系列不同取代的α-硫代酯,得到高达90%的产率。另一方面,在空气下18小时后,使用2当量的碱基,α-硫酮酮。此外,在较短的反应时间之后,可以使酮烯醇互变异构体的分离,揭示它们作为机制阐明的重要中间体。

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