研究简报

四丁基碘化铵催化的sp3-C—H键的磷酸酯化

  • 王倩 ,
  • 徐洲
展开
  • 徐州医学院基础学院生化与化学综合实验室 徐州 221004

收稿日期: 2013-05-30

  修回日期: 2013-07-08

  网络出版日期: 2013-07-11

基金资助

江苏省高校自然科学基金(No. 10KJB150018)资助项目.

Tetrabutylammonium Iodide-Catalyzed Phosphonation of sp3-C—H Bonds

  • Wang Qian ,
  • Xu Zhou
Expand
  • Experimental Center for Biochemistry and Chemistry Teaching, School of Basic Sciences, Xuzhou Medical College, Xuzhou 221004

Received date: 2013-05-30

  Revised date: 2013-07-08

  Online published: 2013-07-11

Supported by

Project supported by the Natural Science Foundation of Higher Education Institutions of Jiangsu Province (No. 10KJB150018).

摘要

以四丁基碘化铵(TBAI)为催化剂,过氧叔丁醇(TBHP)作为氧化剂,在温和的反应条件下实现了叔胺氮的邻位碳原子上sp3-C—H键与亚磷酸酯的氧化偶联,反应条件温和,室温、空气下即可进行,适用范围广泛,产率高,后处理方便. 为新的C—P键的形成提供了一条简洁高效的反应路径,并且合成了一系列可能具有重要药理和生物活性的α-氨基磷酸酯化合物.

本文引用格式

王倩 , 徐洲 . 四丁基碘化铵催化的sp3-C—H键的磷酸酯化[J]. 有机化学, 2013 , 33(11) : 2430 -2434 . DOI: 10.6023/cjoc201305052

Abstract

Activation of sp3-C—H bonds and oxidative phosphonation of sp3-C—H bonds adjacent to a nitrogen atom of tertiary amine were catalyzed by tetrabutylammonium iodide (TBAI) with t-butylhydroperoxide (TBHP) as oxidant under mild reaction conditions. The safe, convenient, and environmentally benign process, as well as the broad substrate scope, low catalyst loading, high selectivity, short reaction time, and good yields make the protocol very practical.

参考文献

[1] (a) Li,Z.; Li,C.J.J.Am.Chem.Soc.2005,127,3672.
(b) Basle,C.; Li,C.J.Green Chem.2007,9,1047.
(c) Boess,E.; Sureshkumar,D.; Sud,A.; Wirtz,C.; Fares,C.; Klussmann,M.J.Am.Chem.Soc.2011,133,8106.
[2] (a) Han,W.; Ofial,A.R.Chem.Commun.2009,5024.
(b) Singhal,S.Jain,S.L.; Sain,B.Chem.Commun.2009,2371.
(c) Zhang,Y.; Peng,H.; Zhang,M.; Cheng,Y.X.; Zhu,C.J.Chem.Commun.2011,2354.
(d) Liu,P.; Liu,Y.; Wong,E.L.M.; Xiang,S.; Che,C.M.Chem.Sci.2011,2,2187.
[3] (a) Yoo,W.J.; Li,C.J.Top.Curr.Chem.2009,292,281.
(b) So,M.H.; Liu,Y.; Ho,C.M.; Che,C.M.Chem.Asian J.2009,4,1551.
[4] (a) Yeung,C.S.; Dong,V.M.Chem.Rev.2011,111,1215.
(b) Sun,C.L.; Li,B.J.; Shi,Z.J.Chem.Rev.2011,111,1293.
[5] (a) Liu,C.; Zhang,H.; Shi,W.; Li,A.Chem.Rev.2011,111,1780.
(b) Li,B.J.; Shi,Z.J.Chem.Soc.Rev.2012,41,5588.
(c) Wang,S.; Li,Y.; Liu,H.C.Acta Chim.Sinica 2012,70,1897 (in Chinese).(王帅; 李洋; 刘海超,化学学报,2012,70,1897.)
(d) Pan,F.; Shi,Z.J.Acta Chim.Sinica 2012,70,1679 (in Chinese).(潘菲,施章杰,化学学报,2012,70,1679.)
(e) Zhang,Z.P.; Yu,H.Z.; Fu,Y.; Guo,Q.X.Acta Chim.Sinica 2011,69,821 (in Chinese).(张志平,于海珠,傅尧,郭庆祥,化学学报,2011,69,821.)
(f) Li,J.S.; Cai,F.F.; Li,Z.W.; Xue,Y.; Cheng,C.; Liu,W.D.; Cao,Z.Chin.J.Chem.2012,30,1699.
[6] (a) Hiratake,J.; Oda,J.Biosci.Biotechnol.Biochem.1997,61,211.
(b) Kafarski,P.; Lejczak,B.Phosphorus,Sulfur Silicon Relat.Elem.1991,63,193.
(c) Gu,L.J.; Wang,R.; Huang,X.Z.; Jin,C.Chin.J.Chem.2012,30,2483.
[7] (a) Pratt,R.F.Science 1989,246,917.
(b) Maier,L.; Diel,P.J.Phosphorus,Sulfur Silicon Relat.Elem.1991,57,57.
[8] (a) Beers,S.A.; Schwender,C.F.; Loughney,D.A.; Malloy,E.; Demarest,K.; Jordan,J.Bioorg.Med.Chem.1996,4,1693.
(b) Vovk,A.I.; Mischenko,I.M.; Tanchuk,V.Y.; KachkovskⅡ,G.A.; Sheiko,S.Y.; Kolodyazhnyi,O.I.; Kukhar,V.P.Bioorg.Med.Chem.2008,18,4620.
[9] (a) Manabe,K.; Kobayashi,S.Chem.Commun.2000,669.
(b) Yadav,J.S.; Reddy,B.V.S.; Raj,K.S.; Reddy,K.B.; Prasad,A.R.Synthesis 2001,2277.
[10] (a) Saidi,M.R.; Azizi,N.Synlett 2002,1347.
(b) Akiyama,T.; Sanada,M.; Fuchibe,K.Synlett 2003,1463.
[11] (a) Han,W.; Ofial,R.Chem.Commun.2009,6023.
(b) Hari,D.P.; Konig,B.Org.Lett.2011,13,3852.
[12] (a) Xue,Q.C.; Xie,J.; Jin,H.M.; Cheng,Y.X.; Zhu,C.J.Org.Biomol.Chem.2013,11,1606.
(b) Rueping,M.; Zhu,S.Q.; Koenigs,R.M.Chem.Commun.2011,47,8679.
(c) Dhineshkumar,J.; Lamani,M.; Alagiri,K.; Prabhu,K.R.Org.Lett.2013,15,1092.
[13] (a) Xie,J.; Li,H.M.; Xue,Q.C.; Cheng,Y.X.; Zhu,C.J.Adv.Synth.Catal.2012,354,1646.
(b) Alagiri,K.; Devadig,P.; Prabhu,K.R.Chem.Eur.J.2012,18,5160.
(c) Alagiri,K.; Devadig,P.; Prabhu,K.R.Tetrahedron Lett.2012,53,1456.
(d) Wang,H.L.; Li,X.C.; Wu,F.; Wan,B.S.Tetrahedron Lett.2012,53,681.
[14] (a) Richardson,R.D.; Wirth,T.Angew.Chem.,Int.Ed.2006,45,4402.
(b) Ochiai,M.; Miyamoto,K.Eur.J.Org.Chem.2008,4229.
(c) Dohi,T.; Kita,Y.Chem.Commun.2009,2073.
[15] Kirihara,M.; Asai,Y.; Ogawa,S.; Noguchi,T.; Hatano,A.; Hirai,Y.Synthesis 2007,3286.
[16] (a) Uyanik,M.; Okamoto,H.; Yasui,T.; Ishihara,K.Science 2010,328,1376.
(b) Uyanik,M.; Ishihara,K.Chim.Oggi 2011,29,18.
(c) Uyanik,M.; Suzuki,D.; Yasui,T.; Ishihara,K.Angew.Chem.,Int.Ed.2011,50,5331.
[17] Chen,L.; Shi,E.; Liu,Z.; Chen,S.; Wei,W.; Li,H.; Xu,K.; Wan,X.Chem.Eur.J.2011,17,4085.
[18] Ma,L.J.; Wang,X.P.; Yu,W.; Han,B.Chem.Commun.2011,47,11333.
[19] Basle,O.; Li,C.J.Chem.Commun.2009,4124.
文章导航

/