Synthesis of 3,5-Diaryl and 3,5-Dialkyl-1,2-dithiolylium-4-olates

D. Barillier
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引用次数: 1

Abstract

Abstract Sulfurization of 2-acetoxy or 2-benzoyloxy-1,3-propanediones gives the corresponding 1,2-dithiolylium salts which are used as starting materials for preparation of 1,2-dithiolylium-4-olates. The reaction was studied under different conditions in order to obtain the best sulfurization yields. A new 3-p-dimethylaminophenyl-5-phenyl-1,2-dithiolylium-4-olate is also described. It is formed by nucleophilic attack on a 3-alkylthio substituted or a 5 unsubstituted position of a 1,2-dithiolylium ion by N, N-dimethylaniline.
3,5-二芳基和3,5-二烷基-1,2-二硫柳酸盐的合成
摘要2-乙酰氧基或2-苯甲酰氧基-1,3-丙二酮经硫化得到相应的1,2-二硫鎓盐,作为制备1,2-二硫鎓-4-酸盐的起始原料。为了获得最佳的硫化产率,在不同条件下对该反应进行了研究。还报道了一种新的3-对-二甲氨基苯基-5-苯基-1,2-二硫柳-4-酸盐。它是由N, N-二甲基苯胺对取代的3-烷基硫基或未取代的5 - 1,2-二硫基离子的亲核攻击形成的。
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