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DOI: 10.1055/s-0031-1289732
Convenient Chlorination of Some Special Aromatic Compounds Using N-Chlorosuccinimide
Publikationsverlauf
Publikationsdatum:
01. März 2012 (online)
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Abstract
Some chlorinated aromatic compounds, including indole, benzofuran, carbazole, pyridine and aniline derivatives, are difficult to obtain through convenient chlorination. We herein report their efficient synthesis through chlorination with N-chlorosuccinimide (NCS). Optimization of the reaction conditions, including the temperature and the choice of solvent, was also investigated. This approach, which is characterized by a facile procedure, comparatively high yields and environmentally friendly features, provides a straightforward and inexpensive route to several chlorinated aromatic compounds.
Key words
chlorination - N-chlorosuccinimide - indoles - benzofurans - carbazoles - pyridines
-
2a
Dewkar GK.Narina SV.Sudalai A. Org. Lett. 2003, 5: 4501 -
2b
Yu G.-X.Mason HJ.Galdi K.Wu X.-M.Cornelius L.Zhao N.Witkus M.Ewing WR.Macor JE. Synthesis 2003, 403 -
2c
Jayachandran B.Phukan P.Daniel T.Sudalai A. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 2006, 45: 972 -
2d
U.S. Statutes. Clean Air Act Amendments of 1990 (Public Law 101-549).
-
3a
Nickson TE.Roche-Dolson CA. Synthesis 1985, 669 -
3b
Bovonsombat P.Ali R.Khan C.Leykajarakul J.Pla-on K.Aphimanchindakul S.Pungcharoenpong N.Timsuea N.Arunrat A.Punpongjareorn N. Tetrahedron 2010, 66: 6928 -
3c
Yamamoto T.Toyota K.Morita N. Tetrahedron Lett. 2010, 51: 1364 - 4
Zysman-Colman E.Arias K.Siegel JS. Can. J. Chem. 2009, 87: 440 - 5
Bartoli S.Cipollone A.Squarcia A.Madami A.Fattori D. Synthesis 2009, 1035 - 6
Surya Prakash GK.Mathew T.Hoole D.Esteves PM.Wang Q.Rasul G.Olah GA. J. Am. Chem. Soc. 2004, 126: 15770 - 7
Kunzer AR.Wendt MD. Tetrahedron Lett. 2011, 52: 1815 -
8a
Showalter HDH.Sercel AD.Leja BM.Wolfangel CD.Ambroso LA.Elliott WL.Fry DW.Kraker AJ.Howard CT.Lu GH.Moore CW.Nelson JM.Roberts BJ.Vincent PW.Denny WA.Thompson AM. J. Med. Chem. 1997, 40: 413 -
8b
Marchetti L.Andreani A. Ann. Chim. (Rome) 1973, 63: 681 -
9a
Tang S.Li J.-H.Xie Y.-X.Wang N.-X. Synthesis 2007, 1535 -
9b
Yamada K.Kanbayashi Y.Tomioka S.Somei M. Heterocycles 2002, 57: 1627 - 10
Bogdal D.Lukasiewicz M.Pielichowski J. Green Chem. 2004, 6: 110 - 11
Bowyer PM.Iles DH.Ledwith A. J. Chem. Soc. C 1971, 2775 - 12
Bonesi MS.Erra-Balsells R. J. Heterocycl. Chem. 1997, 34: 877 - 13
Orlov VY.Begunov RS.Demidova NY.Rusakov AI. Russ. J. Gen. Chem. 2006, 76: 76 - 14
Sonavane SU.Jayaram RV. Synth. Commun. 2003, 33: 843 - 15
Farhadi S.Kazem M.Siadatnasab F. Polyhedron 2011, 30: 606 - 16
Mohapatra SK.Sonavane SU.Jayaram RV.Selvam P. Tetrahedron Lett. 2002, 43: 8527 - 17
Farhadi S.Siadatnasab F. J. Mol. Catal. A: Chem. 2011, 339: 108 - 18
Stokes BJ.Jovanovic B.Dong H.-J.Richert KJ.Riell DR.Driver TG. J. Org. Chem. 2009, 74: 3225 - 19
Kalatzis E.Mastrokalos C. J. Chem. Soc., Perkin Trans. 2 1977, 1835 - 20
Raju RR.Mohan SK.Reddy SJ. Tetrahedron Lett. 2003, 44: 4133 - 21
Talik T. Rocz. Chem. 1963, 37: 69 - 22
Crowther AF.Curd FHS.Davey DG.Hendry JA.Hepworth W.Rose FL. J. Chem. Soc. 1951, 1774 - 23
Sbarbati NE. J. Org. Chem. 1965, 30: 3365
References
These authors contributed equally to this work.