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由不同硫含氧酸盐引发的氟烷基化内酯化反应

Polyfluoroalkylation Lactonization Initiated by Sulfur-oxy Acid Salts
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摘要 以4-氯八氟碘代丁烷和4-戊烯酸生成含氟丁内酯的反应为模板,详细研究了不同硫含氧酸盐、溶剂和温度对反应的影响。实验结果表明:以二氧化硫脲、雕白粉、亚硫酸钠、亚硫酸氢钠、偏重亚硫酸钠等硫含氧酸盐为引发剂,4-氯八氟碘代丁烷和4-戊烯酸的氢氧化钠水溶液与乙腈或DMF为共溶剂,于20~55°C搅拌反应3~15h,后处理并通过柱层析得到含氟内酯产物。以二氧化硫脲为引发剂,乙腈为共溶剂(V(乙腈)∶V(水)=1∶1),在35°C下反应5h,得到的含氟内酯产率最高(84.3%)。在此条件下,其他含氟碘代烷与4-戊烯酸反应,得到相应的含氟内酯化合物,收率为72.7%~86.2%。 The polyfluoroalkylation lactonization of 4-pentenoic acid with 4-chlorododecafluorobutyl iodide initiated by several sulfur-oxy acid salts, such as thiourea dioxide, rongalite, sodium sulfite, sodium bisulfite and sodium disulfite, to give the correponding fluorine-containing lactones was intensively studied. The influence of temperature, time and cosolvent on the reaction was discussed. Results show that lactone is obtained after usual workup when the mixture of 4-pentenoic acid and 4-chlorodode-cafluorobutyliodide are stirred in the presence of different sulfur-oxy acid salts at 20-55°C for 3-15 h in aqueous acetonitrile (or DMF) solution. When the reaction was initiated by thiourea dioxide at 35°C for 5 h in aqueous acetonitrile solution the yield was the highest (84.3%). Polyfluoroalkylated lactones can be obtained in 72.7%-86.2% yields by reaction of 4-pentenoic acid and polyfluoroalkyl iodides under similar conditions.
出处 《华东理工大学学报(自然科学版)》 EI CAS CSCD 北大核心 2005年第3期339-341,370,共4页 Journal of East China University of Science and Technology
基金 国家自然科学基金资助项目(29902001)
关键词 4-戊烯酸 硫含氧酸盐 Γ-丁内酯 氟烷基化内酯化反应 4-pentenoic acid sulfur-oxy acid salts γ-butyrolactones polyfluoroalkylation (lactonization)
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参考文献5

  • 1Ramachandran P V, Padiya K J, Rauniyar V, et al. Asymmetric synthesis of γ-perfluoro-alkyl(ary1) butyrolactones via organoboranes[J]. Tetrahedron Lett, 2004, 45(5):1 015-1 017.
  • 2石川延男.含氟生理活性物质的开发和应用[M].上海:华东理工大学出版社,2001.1-3.
  • 3Brace N O. Syntheses with perfluoroalkyl radicals from perfluoroalkyl iodides: A rapid survey of synthetic possibilities with emphasis on practical applications. Part one: Alkenes, alkynes and allylic compounds[J]. J Fluorine Chem, 1999, 93(1):1-25.
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