%0 Journal Article %T 应用量子化学反应性指数分析4,4-二苯丁腈的合成
Analyzing the Synthesis of 4,4-Diphenylbutyronitrile by Quantum Chemical Reactivity Index %A 李彤 %A 雷滨瑜 %A 闵清 %A 邵开元 %A 胡文祥 %J Journal of Comparative Chemistry %P 1-11 %@ 2574-4135 %D 2024 %I Hans Publishing %R 10.12677/cc.2024.81001 %X 4,4-二苯丁腈是合成H1受体激动剂Histaprodifens的重要原料之一。化学结构虽然简单,但合成它,要么合成方法简单但需要昂贵的原材料,要么原材料虽然便宜但合成条件苛刻。为了改进4,4-二苯丁腈的合成工艺,我们采用较为便宜的原材料,并通过量子化学计算获得反应的化学反应性指数,来研究和探讨反应机制并指导实验操作。本文在传统的用金属钾对二苯甲烷的烷烃基拔氢反应的方法基础上,采用间接法,即以四甲基乙二胺为起始原料,与正丁基锂发生偶合反应,形成四甲基乙二胺锂鎓盐;后再与二苯甲烷反应,形成二苯甲烷锂盐,最后与3-溴丙腈反应,完成4,4-二苯丁腈的制备。实验表明,该反应条件温和,原料易得,成本低且对环境较友好,反应总收率可达80%左右;实验表明,采用量子化学反应性指数可以分析反应的全过程,并成功地指导化学反应的操作过程。
4,4-diphenylbutyronitrile is a crucial raw material for synthesizing H1 receptor agonist Histaprodifens. Despite its simple chemical structure, the synthesis process requires either expensive raw materials or harsh reaction conditions when using cheaper alternatives. To improve the synthesis of 4,4-diphenylbutyronitrile, we utilized quantum chemistry calculations to determine the chemical reactivity index and guide experimental operations while using cost-effective starting materials. In this study, we employed an indirect method based on traditional alkane hydrogen extraction reactions with metal potassium on diphenylmethane. Specifically, tetramethyl ethylenediamine was used as a starting material and combined with n-butyllithium to form N,N,N',N'-tetramethylethylenediamine lithium salt before reacting with diphenylmethane to produce diphenylmethane lithium salt. Finally, 3-bromopropionitrile was added to complete the preparation of 4,4-diphenylbutyronitrile. The results showed that this mild reaction-n condition utilizing easily obtainable raw materials had low costs and environmental impact while achieving a total yield of up to 80%. Furthermore, our experiment demonstrated that analyzing the entire reaction process through quantum chemical reactivity index could successfully guide operational procedures. %K 4 %K 4-二苯丁腈,量子化学,反应性指数,合成
4 %K 4-Diphenylbutyronitrile %K Quantum Chemistry %K Reactivity Index %K Synthesis %U http://www.hanspub.org/journal/PaperInformation.aspx?PaperID=88768