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Synthesis of Dibenzyl Thioether using H2S and Anion Exchange Resin as Triphase Catalyst

机译:硫化氢和阴离子交换树脂为三相催化剂合成二苄基硫醚

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摘要

This study focuses on the utilization of Hydrogen Sulphide (H2S) for the synthesis of Dibenzyl Sulphide (DBS) and Benzyl Mercaptan (BM). This involves first the absorption of H2S in mono Ethanolamine and then reaction of this H2S rich mono Ethanolamine with Benzyl Chloride for the synthesis of DBS and BM. The mono Ethanolamine and Benzyl Chloride are two different phases and their reaction is very difficult. So to carry out this reaction a phase transfer catalyst has been used. The Amberlite IR400 has been chosen as the phase transfer catalyst as it is solid and can be reused. The objective of this work is to maximize the conversion of Benzyl Chloride and maximize the selectivity of DBS. In this work the Benzyl Chloride has been used along with Toluene as a solvent. In the system under study, conversion of maximum of 90% was obtained and the desired product was obtained with 46% selectivity. Reaction time, catalyst loading, stirring speed, initial sulphide concentration and Benzyl Chloride concentration are chosen as parameters.
机译:这项研究的重点是利用硫化氢(H2S)合成二苄基硫化物(DBS)和苄基硫醇(BM)。这包括首先在单乙醇胺中吸收H2S,然后使这种富含H2S的单乙醇胺与苄基氯反应生成DBS和BM。一元乙醇胺和氯化苄是两个不同的相,它们的反应非常困难。因此为了进行该反应,已经使用了相转移催化剂。由于Amberlite IR400固体且可以重复使用,因此已被选作相转移催化剂。这项工作的目的是使苄基氯的转化率最大化,并使DBS的选择性最大化。在这项工作中,苄基氯已与甲苯一起用作溶剂。在研究的系统中,最大转化率为90%,选择性为46%,得到了所需的产物。选择反应时间,催化剂负载量,搅拌速度,初始硫化物浓度和苄基氯浓度作为参数。

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    Vikash Kumar;

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  • 年度 2012
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