首页> 外文期刊>Russian Journal of Organic Chemistry >Unexpected Formation of 1,6-Bis[3,5-dimethyl-4-(1,4,6-oxa-dithiocan-5-yl)-1H-pyrazol-1-yl]hexane in the Reaction of 1,1'-(Hexane-1,6-diyl)bis[3,5-dimethyl-1H-pyrazole-4-carbaldehyde]with 2-Sulfanylethanol
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Unexpected Formation of 1,6-Bis[3,5-dimethyl-4-(1,4,6-oxa-dithiocan-5-yl)-1H-pyrazol-1-yl]hexane in the Reaction of 1,1'-(Hexane-1,6-diyl)bis[3,5-dimethyl-1H-pyrazole-4-carbaldehyde]with 2-Sulfanylethanol

机译:1,1'反应中意外生成1,6-双[3,5-二甲基-4-(1,4,6-氧杂二硫代-5-基)-1H-吡唑-1-基]己烷-(己烷-1,6-二基)双[3,5-二甲基-1H-吡唑-4-甲醛)与2-硫烷基乙醇

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摘要

We previously reported that reactions of aldehydes of the thiophene series[1-3]with alkanethiols and dithiols in the presence of chloro(trimethyl)silane Me3SiCl at reduced temperature provide a simple and convenient synthetic route to acyclic and cyclic dithio-acetals possessing thiophene fragments.It is also known that 2-sulfanylethanol and 3-sulfanylpropan-1-ol react with aliphatic and aromatic aldehydes in the presence of scandium trifluoromethanesulfonate[4],boron trifluoride[5],or p-toluenesulfonic acid[6]to give the corresponding 1,3-oxathiolane and 1,3-oxa-thiane derivatives.
机译:我们以前曾报道过,噻吩系列[1-3]的醛与链烷硫醇和二硫醇在氯(三甲基)硅烷Me3SiCl的存在下,在较低的温度下反应,提供了一种简单且方便的合成路线,以合成具有噻吩片段的无环和环状二硫代缩醛还已知在三氟甲烷磺酸scan [4],三氟化硼[5]或对甲苯磺酸[6]存在下,2-硫烷基乙醇和3-硫烷基丙烷-1-醇与脂肪族和芳香族醛反应。相应的1,3-氧杂硫杂环戊烷和1,3-氧杂噻吩衍生物。

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