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Applying the principles of green chemistry to selected traditional organic chemistry reactions

机译:将绿色化学原理应用于选定的传统有机化学反应

摘要

The primary objective of this project was to apply the principles of green chemistry to selected traditional synthetic organic chemistry reactions. The reactions studied in the lab were: amide formation, oxidation of alcohols with KMnO4 and LiCl/H2O2, oxidation of alkylarenes with KMnO4, reduction of β-ketoesters with yeast, and formation of esters by phase transfer catalysis. Microwave irradiation, biocatalysis, phase transfer catalysis, solvent-free conditions, and/or alternate solvents were used to accomplish these syntheses. Results were analyzed by the traditionally used percent yield calculations and selected green chemistry metrics. The main limitation of the results was that most products were not completely purified due to time constraints.udFor amidification it was found that results obtained using a commercial oven were better than results obtained using a domestic oven. Oxidation with KMnO4 gave higher yields at one week reaction time under solvent-free conditions than under reflux in dichloromethane for 1.5 h. The catalytic oxidation procedure using LiCl/H2O2 was found to be more wasteful than the stoichiometric procedure using KMnO4. Both methods showed preference for oxidation at benzylic as opposed to aliphatic positions. For the oxidation of alkylarenes it was found that dimethylcarbonate is not a suitable replacement for dichloromethane as an extraction solvent in this procedure. Also, higher yields were obtained at one week reaction time under solvent-free conditions than under reflux in dichloromethane for 1.5 h. product analysis for reduction of β-keotesters with yeast tend to suggest that steric factors may play a large role in the reaction with more sterically hindered substrates giving lower yields. Further work in this area is required to elucidate this hypothesis. Only a few esterification reactions were carried out but two of three results gave decent E-factors. Finally, it was shown that the majority of waste from each reaction was from the use of solvent. Therefore, recycling the solvent can have the biggest impact on reducing waste. ud
机译:该项目的主要目的是将绿色化学原理应用于某些传统的合成有机化学反应。在实验室中研究的反应是:酰胺形成,用KMnO4和LiCl / H2O2氧化醇,用KMnO4氧化烷基芳烃,用酵母还原β-酮酸酯和通过相转移催化形成酯。微波辐射,生物催化,相转移催化,无溶剂条件和/或替代溶剂用于完成这些合成。通过传统上使用的百分比产率计算和选定的绿色化学指标对结果进行分析。结果的主要限制是由于时间限制,大多数产品未完全纯化。 udd对于酰胺化,发现使用商用烤箱获得的结果优于使用家用烤箱获得的结果。与在二氯甲烷中回流1.5小时相比,在无溶剂条件下,用KMnO4氧化在一周的反应时间内可获得更高的产率。发现使用LiCl / H2O2的催化氧化过程比使用KMnO4的化学计量过程更浪费。与脂族位置相反,两种方法均显示出优选在苄基上进行氧化。对于烷基芳烃的氧化,发现在该方法中碳酸二甲酯不适合代替二氯甲烷作为萃取溶剂。同样,在无溶剂条件下,在一周的反应时间获得的产率高于在二氯甲烷中回流1.5小时的产率。用酵母还原β-keotesters的产物分析倾向于表明,空间位阻可能在反应中起较大作用,受空间位阻更大的底物产生的产率较低。为了阐明这一假设,需要在这一领域做进一步的工作。仅进行了少量酯化反应,但三个结果中的两个给出了不错的E因子。最后,结果表明,每个反应产生的大部分废料来自溶剂的使用。因此,回收溶剂对减少废物的影响最大。 ud

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    White Steven D.;

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  • 年度 2013
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