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首页> 外文期刊>Beilstein journal of organic chemistry. >Selective synthesis of α-organylthio esters and α-organylthio ketones from β-keto esters and sodium S-organyl sulfurothioates under basic conditions
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Selective synthesis of α-organylthio esters and α-organylthio ketones from β-keto esters and sodium S-organyl sulfurothioates under basic conditions

机译:在碱性条件下选择性合成β-酮酯和S-氧化钠硫核酸钠的α-氧化酯和α-氧化钠酮

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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通过在甲苯的基本条件下在甲苯的基本条件下将β-酮酯与S-苄基磺基硫代钠或S-烷基磺基硫代钠(Bunte Salts)的反应制备α-氧化酯酯和α-氧化硫硫基酮的选择性方法。 在使用4当量的碱的时,获得一系列不同取代的α-硫酯,得到高达90%的产率。另一方面,采用2当量的碱,α-硫酮酮在后 在空气下18小时。在反应时间较短的情况下,可以将酮-EnOL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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