节点文献
由芳基炔基硒醚与对甲苯磺酸反应制备芳基硒代羧酸酯
Synthesis of Aryl Selenoesters by Reaction of Alkynyl Aryl Selenide and p-Toluenesulfonic Acid
【摘要】 端炔、二醋酸碘苯和二芳基二硒醚于二氯甲烷溶剂中制得芳基炔基硒醚,再将芳基炔基硒醚和对甲苯磺酸在二氯甲烷中加热回馏,冷却后加入适量水即可一锅法制得芳基硒代羧酸酯.该法具有原料易得、反应条件温和、操作方便和产率较高(70%~81%)等优点.
【Abstract】 Alkynyl aryl selenides were prepared from the reaction of terminal alkynes with iodobenzene diacetate and diaryl selenides in methylene chloride at 0 ℃.A mixture of the alkynyl aryl selenide and p-toluenesulfonic acid in methylene chloride was refluxed for 4 h,cooled, and then treated with water to afford aryl selenoesters. This one-pot synthetic procedure of aryl selenoester has the advantage of ready availability of starting materials, mild reaction condition, convenient manipulation and good yields (70%~81%).
【关键词】 芳基硒代羧酸酯;
一锅法;
芳基炔基硒醚;
合成;
【Key words】 aryl selenoester; alkynyl aryl selenide; one-pot synthetic method;
【Key words】 aryl selenoester; alkynyl aryl selenide; one-pot synthetic method;
【基金】 江西省自然科学基金资助课题(020512)
- 【文献出处】 江西师范大学学报(自然科学版) ,Journal of Jiangxi Normal University (Natural Sciences Edition) , 编辑部邮箱 ,2003年02期
- 【分类号】O627.6
- 【被引频次】2
- 【下载频次】84