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作 者:Yu,Haifeng
机构地区:[1]Department of Chemistry,Anshan Normal University,Anshan,Liaoning 114007,China
出 处:《Chinese Journal of Chemistry》2012年第2期367-371,共5页中国化学(英文版)
基 金:This work was supported by the National Natural Science Foundation of China (No. 20572013) and the Doctoral Foundation of Anshan Normal University.
摘 要:Using 2-[bis(alkylthio)methylene]-3-oxo-N-o-tolylbutanamides 1 as odorless thiol equivalents, an efficient and odorless synthesis of thioethers has been developed. Promoted by NaOH in EtOH, the cleavage of 1 commences to generate thiolate anions, and the generated thiolate anions then react with halides to give various thioethers in good yield. It is noteworthy that only a very faint odor ofthiols can be perceived during both the reaction and the workup.Using 2-[bis(alkylthio)methylene]-3-oxo-N-o-tolylbutanamides 1 as odorless thiol equivalents, an efficient and odorless synthesis of thioethers has been developed. Promoted by NaOH in EtOH, the cleavage of 1 commences to generate thiolate anions, and the generated thiolate anions then react with halides to give various thioethers in good yield. It is noteworthy that only a very faint odor ofthiols can be perceived during both the reaction and the workup.
关 键 词:a-oxo-ketene dithioacetals odorless thiols equivalents THIOETHERS HALIDES
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