Synthesis 2018; 50(13): 2555-2566
DOI: 10.1055/s-0037-1609687
paper
© Georg Thieme Verlag Stuttgart · New York

A Novel Method for the Chlorolactonization of Alkenoic Acids Using Diphenyl Sulfoxide/Oxalyl Chloride

Rui Ding
Beijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing Key Laboratory of Flavor Chemistry, Beijing Technology and Business University, 100048 Beijing, P. R. of China   Email: tianhy@btbu.edu.cn   Email: sunbg@btbu.edu.cn
,
Liyuan Lan
Beijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing Key Laboratory of Flavor Chemistry, Beijing Technology and Business University, 100048 Beijing, P. R. of China   Email: tianhy@btbu.edu.cn   Email: sunbg@btbu.edu.cn
,
Shuhui Li
Beijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing Key Laboratory of Flavor Chemistry, Beijing Technology and Business University, 100048 Beijing, P. R. of China   Email: tianhy@btbu.edu.cn   Email: sunbg@btbu.edu.cn
,
Yongguo Liu
Beijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing Key Laboratory of Flavor Chemistry, Beijing Technology and Business University, 100048 Beijing, P. R. of China   Email: tianhy@btbu.edu.cn   Email: sunbg@btbu.edu.cn
,
Shaoxiang Yang
Beijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing Key Laboratory of Flavor Chemistry, Beijing Technology and Business University, 100048 Beijing, P. R. of China   Email: tianhy@btbu.edu.cn   Email: sunbg@btbu.edu.cn
,
Hongyu Tian*
Beijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing Key Laboratory of Flavor Chemistry, Beijing Technology and Business University, 100048 Beijing, P. R. of China   Email: tianhy@btbu.edu.cn   Email: sunbg@btbu.edu.cn
,
Baoguo Sun*
Beijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing Key Laboratory of Flavor Chemistry, Beijing Technology and Business University, 100048 Beijing, P. R. of China   Email: tianhy@btbu.edu.cn   Email: sunbg@btbu.edu.cn
› Author Affiliations
Financial support from the National Key Research and Development Program (2016YFD0400801), Beijing Postdoctoral Research Foundation (2017-22-011), and the Importation and Development of High-Caliber Talents Project of Beijing Municipal Institutions (CIT&TCD20140306) is gratefully acknowledged.
Further Information

Publication History

Received: 28 February 2018

Accepted after revision: 22 March 2018

Publication Date:
24 April 2018 (online)


Abstract

A facile chlorolactonization of alkenoic acids by treatment with diphenyl sulfoxide/oxalyl chloride has been developed. The reaction can generate various chlorolactones in moderate to good yields, wherein the chlorodiphenylsufonium salt derived from diphenyl sulfoxide/oxalyl chloride serves as the source of Cl+.

Supporting Information

 
  • References

    • 1a Nolsøe JM. J. Hansen TV. Eur. J. Org. Chem. 2014; 3051
    • 1b Murai K. Fujioka H. Heterocycles 2013; 87: 763
    • 1c Laya MS. Banerjee AK. Cabrera EV. Curr. Org. Chem. 2009; 13: 720
    • 1d Ranganathan S. Muraleedharan KM. Vaish NK. Jayaraman N. Tetrahedron 2004; 60: 5273
    • 1e Dowle MD. Davies DI. Chem. Soc. Rev. 1979; 8: 171
    • 1f Bougault MJ. Ann. Chim. Phys. 1908; 14: 145
    • 1g Fittig R. Justus Liebigs Ann. Chem. 1904; 331: 88
    • 1h Stobbe H. Justus Liebigs Ann. Chem. 1902; 321: 83
    • 2a Tănase CI. Drăghici C. Shova S. Cojocaru A. Maganu M. Munteanu CV. A. Cocu F. Tetrahedron 2015; 71: 6852
    • 2b Gładkowski W. Skrobiszewski A. Mazur M. Siepka M. Pawlak A. Obmińska-Mrukowicz B. Białońska A. Poradowski D. Drynda A. Urbaniak M. Tetrahedron 2013; 69: 10414
    • 3a Kobayashi S. Yokoi T. Inoue T. Hori Y. Saka T. Shimomura T. Masuyama A. J. Org. Chem. 2016; 81: 1484
    • 3b Wilking M. Daniliuc CG. Hennecke U. Chem. Eur. J. 2016; 22: 18601
    • 3c Wong Y.-C. Yeung Y.-Y. Org. Biomol. Chem. 2016; 14: 3202
    • 3d Mellegaard-Waetzig SR. Wang C. Tunge JA. Tetrahedron 2006; 62: 7191
    • 3e Mellegaard SR. Tunge JA. J. Org. Chem. 2004; 69: 8979
    • 4a Aursnes M. Tungen JE. Hansen TV. J. Org. Chem. 2016; 81: 8287
    • 4b Gelat F. Coffinet M. Lebrun S. Agbossou-Niedercorn F. Michon C. Deniau E. Tetrahedron: Asymmetry 2016; 27: 980
    • 5a Bennett SM. Tang Y. McMaster D. Bright FV. Detty MR. J. Org. Chem. 2008; 73: 6849
    • 5b Goodman MA. Detty MR. Organometallics 2004; 23: 3016
    • 5c Drake MD. Bateman MA. Detty MR. Organometallics 2003; 22: 4158
    • 6a Denmark SE. Ryabchuk P. Burk MT. Gilbert BB. J. Org. Chem. 2016; 81: 10411
    • 6b Yousefi R. Ashtekar KD. Whitehead DC. Jackson JE. Borhan B. J. Am. Chem. Soc. 2013; 135: 14524
    • 6c Zhang W. Liu N. Schienebeck CM. Decloux K. Zheng S. Werness JB. Tang W. Chem. Eur. J. 2012; 18: 7296
    • 6d Yousefi R. Whitehead DC. Mueller JM. Staples RJ. Borhan B. Org. Lett. 2011; 13: 608
    • 6e Whitehead DC. Yousefi R. Jaganathan A. Borhan B. J. Am. Chem. Soc. 2010; 132: 3298
    • 7a Zhu M. Li L. Tong JY. Zhang H. Chin. Chem. Lett. 2011; 22: 431
    • 7b López-López JA. Guerra FM. Moreno-Dorado FJ. Jorge ZD. Massanet GM. Tetrahedron Lett. 2007; 48: 1749
    • 8a Abe H. Fukazawa N. Kobayashi T. Ito H. Tetrahedron 2013; 69: 2519
    • 8b Genovese S. Epifano F. Pelucchini C. Procopio A. Curini M. Tetrahedron Lett. 2010; 51: 5992
  • 9 Damin B. Forestiere A. Garapon J. Sillion B. J. Org. Chem. 1981; 46: 3552
  • 10 Zhang T. Dai Y. Cheng S. Liu Y. Yang S. Sun B. Tian H. Synthesis 2017; 49: 1380
  • 11 Denmark SE. Edwards MG. J. Org. Chem. 2006; 71: 7293
  • 12 Krehl S. Geissler D. Hauke S. Kunz O. Staude L. Schmidt B. Beilstein J. Org. Chem. 2010; 6: 1188
  • 13 Muratore ME. Holloway CA. Pilling AW. Storer RI. Trevitt G. Dixon DJ. J. Am. Chem. Soc. 2009; 131: 10796
  • 14 Demertzidou VP. Pappa S. Sarli V. Zografos AL. J. Org. Chem. 2017; 82: 8710
  • 15 Jadhav SB. Ghosh U. Tetrahedron Lett. 2007; 48: 2485
  • 16 Garratt DG. Ryan MD. Beaulieu PL. J. Org. Chem. 1980; 45: 839