Synthesis 2012; 44(8): 1159-1162
DOI: 10.1055/s-0031-1290578
special topic
© Georg Thieme Verlag Stuttgart · New York

Convenient Chlorination with Concentrated Hydrochloric Acid in the Presence of Iodosylbenzene

Tsugio Kitamura*
Department of Chemistry and Applied Chemistry, Graduate School of Science and Engineering, Saga University, Honjo-machi, Saga 840-8502, Japan, Fax: +81(952)288548   Email: kitamura@cc.saga-u.ac.jp
,
Yui Tazawa
Department of Chemistry and Applied Chemistry, Graduate School of Science and Engineering, Saga University, Honjo-machi, Saga 840-8502, Japan, Fax: +81(952)288548   Email: kitamura@cc.saga-u.ac.jp
,
Mohammad Hasan Morshed
Department of Chemistry and Applied Chemistry, Graduate School of Science and Engineering, Saga University, Honjo-machi, Saga 840-8502, Japan, Fax: +81(952)288548   Email: kitamura@cc.saga-u.ac.jp
,
Soichi Kobayashi
Department of Chemistry and Applied Chemistry, Graduate School of Science and Engineering, Saga University, Honjo-machi, Saga 840-8502, Japan, Fax: +81(952)288548   Email: kitamura@cc.saga-u.ac.jp
› Author Affiliations
Further Information

Publication History

Received: 17 February 2012

Accepted: 20 February 2012

Publication Date:
22 March 2012 (online)


Abstract

An efficient chlorination of β-keto esters, 1,3-diketones, and alkenes was performed conveniently with concentrated HCl in the presence of PhIO, selectively giving α-chloro-β-keto esters, 2-chloro-1,3-diketones, and 1,2-dichloroalkanes, respectively. It was suggested that the chlorination took place with (dichloroiodo)benzene generated in situ. A selective anti-addition was observed in the chlorination of indene.

 
  • References

    • 1a Hudlicky M, Hudlicky T In The Chemistry of Halides, Pseudo-Halides and Azides, Supplement D . Patai S, Rappaport Z. Wiley; Chichester: 1983. Chap. 22
    • 1b Sandler SR, Karo W. Organic Functional Group Preparations . 2nd ed. Academic Press; New York: 1983: Chap. 6
    • 1c Larock RC. Comprehensive Organic Transformations . 2nd ed. Wiley-VCH; New York: 1999
    • 2a Varvoglis A. Hypervalent Iodine in Organic Synthesis . Academic Press; New York: 1997
    • 2b Zhdankin VV, Stang PJ. Chem. Rev. 2008; 108: 5299 , and references cited therein
  • 3 Lucas HJ, Kennedy ER. Org. Synth. Coll. Vol. 3 . Wiley; New York: 1955. 482-48
  • 4 Kitamura T, Kuriki S, Morshed MH, Hori Y. Org. Lett. 2011; 13: 2392
    • 5a Zefirov NS, Safronov SO, Kaznacheev AA, Zhdankin VV. Zh. Org. Khim. 1989; 25: 1807
    • 5b Salamant W, Hulme C. Tetrahedron Lett. 2006; 47: 605
  • 6 Heasley GE, Bower TR, Doughharty KW, Easdon JC, Heasley VL, Arnold S, Carter TL, Yaeger DB, Gipe BT, Shellhamer DF. J. Org. Chem. 1980; 45: 5150
    • 7a Podgoršek A, Jurisch M, Stavber S, Zupan M, Iskra J, Gladysz JA. J. Org. Chem. 2009; 74: 3133
    • 7b Chen J.-M, Zeng X.-M, Middleton K, Zhdankin VV. Tetrahedron Lett. 2011; 52: 1952
  • 8 Frantz R, Hintermann L, Perseghini M, Broggini D, Togni A. Org. Lett. 2003; 5: 1709
  • 9 Mei Y, Bentley PA, Du J. Tetrahedron Lett. 2008; 49: 3802
  • 10 Perrone MG, Santandrea E, Dell’Uomo N, Giannessi F, Milazzo FM, Sciarroni AF, Scilimati A, Tortorella V. Eur. J. Med. Chem. 2005; 40: 143
  • 11 Takeda A, Amano E, Tsuboi S. Bull. Chem. Soc. Jpn. 1977; 50: 2191
  • 12 Roshchupkina GI, Gatilov YV, Rybalova TV, Reznikov VA. Eur. J. Org. Chem. 2004; 1765
  • 13 Iranpoor N, Firouzabadi H, Aghapour G, Nahid A. Bull. Chem. Soc. Jpn. 2004; 77: 1885
  • 14 Kamigata N, Satoh T, Yoshida M. Bull. Chem. Soc. Jpn. 1988; 61: 449
  • 15 Adam W, Mock-Knoblauch C, Saha-Moeller CR, Herderich M. J. Am. Chem. Soc. 2000; 122: 9685