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莫达非尼的合成研究

Research on the Synthesis of Modafinil
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摘要 以二苯甲酮(2)为起始原料,经硼氢化钠还原后与五水硫代硫酸钠和氯乙酰胺反应生成Bunte盐缩合得中间体4,4经氧化后得到莫达非尼(1)。产物经^(1)H NMR和MS分析确证,总收率达87%。反应条件温和,收率较高,操作简便,适于工业化生产。 An intermediate■was obtained from the condensation of reduced diphenylmethanone■with Bunte salt formed from the reaction between sodium thiosulfate pentahydrate and chloroacetamide.The target compound1with an overall yield of 87%was obtained from the oxidation reaction of■while the structure of the product was characterized by^(1)H NMR and MS.The advantages of this method include mild reaction condition,satisfactory yields and easy operation.Therefore it will be a promising method for industry.
作者 吴伟杰 李雨轩 徐彩彩 叶海伟 周丽萍 WU Wei-jie;LI Yu-xuan;XU Cai-cai;YE Hai-wei;ZHOU Li-ping(Chemical Pharmaceutical Research Institute,Taizhou Vocational&Technical College,Taizhou 318000,China)
出处 《精细化工中间体》 CAS 2022年第2期24-26,73,共4页 Fine Chemical Intermediates
基金 浙江省大学生科技创新项目(2020R469004) 浙江省教育厅高等学校访问工程师校企合作项目(FG2020223) 浙江省教育厅一般科研项目(Y202147360) 台州职业技术学院“匠心精诚”名班主任工作室阶段性成果。
关键词 莫达非尼 Bunte盐 氧化反应 合成 Modafinil Bunte salt oxidation reaction synthesis
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