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Isolation, synthesis and optimization of cyclopropanation process of 4-allyl-2-methoxyphenol

机译:4-烯丙基-2-甲氧基苯酚的环丙烷化反应的分离,合成与优化

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The synthesis of 4-((2,2-dichlorocyclopropyl)methyl)-2-methoxyphenol 2 have been accomplished by using cyclopropanation process and Reponse Surface Methodology [1,2]. This methodology was used to determine the optimal conditions for the cyclopropanation reaction of eugenol 1. The reaction time (X1) and the ratio of the reaction mixture’s solvent (X2) were the two investigated factors. The statistical analysis of this study indicates that both of these factors had significant effects on the cyclopropanation yield. The central composite design showed that polynomial regression models were in good agreement with the experimental results of the coefficient determination (0.95) of product 2 yield. The optimal conditions were 17.44 and 5.78 hours. In such condition, the predicted yield of the product 2 was 43.96%.
机译:4-((2,2-二氯环丙基)甲基)-2-甲氧基苯酚2的合成已通过使用环丙烷化工艺和响应表面方法[1,2]完成。该方法用于确定丁香酚1的环丙烷化反应的最佳条件。反应时间(X1)和反应混合物溶剂的比例(X2)是两个研究因素。这项研究的统计分析表明,这两个因素均对环丙烷化收率有重大影响。中央复合设计表明,多项式回归模型与产品2产量的系数确定(0.95)的实验结果非常吻合。最佳条件是17.44和5.78小时。在这种条件下,产物2的预测产率为43.96%。

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