Synlett 2011(14): 2069-2071  
DOI: 10.1055/s-0030-1261178
LETTER
© Georg Thieme Verlag Stuttgart ˙ New York

Hypochlorite-Induced Ipso-Substitution Reactions of Aromatic Alcohols and Related Compounds

Hector V. Carrilloa, Angelica Y. Rodrigueza, Robert G. Landolt*a, William H. Hendricksonb
a Department of Chemistry, Texas Wesleyan University, Fort Worth, TX 76105, USA
Fax: +1(871)5314275; e-Mail: rlandolt@txwes.edu;
b Department of Chemistry, University of Dallas, Irving, TX 75062, USA
Further Information

Publication History

Received 13 May 2011
Publication Date:
10 August 2011 (online)

Abstract

Organic solvent extracts derived from aqueous hypochlorite/phase-transfer catalyst solutions induce rapid and efficient ipso substitution of aromatic carbinols and related substrates. The key parameter impacting rates and yields is pH of the original hypochlorite/phase-transfer catalyst component.

    References and Notes

  • 1a Skarzewski J. Siedlecka R. Org. Prep. Proced. Int.  1992,  24:  623 ; this excellent review focuses on advances made through phase-transfer and other catalytic technologies
  • 1b Sakai A. Hendrickson DG. Hendrickson WH. Tetrahedron Lett.  2000,  41:  2759 ; and references cited therein
  • 1c Hill JW. Jenson JA. Henke CF. Yaritz JG. Pedersen RL. J. Chem. Educ.  1984,  61:  1118 
  • 2a Fonouni HE. Krishnan S. Kuhn DG. Hamilton GA. J. Am. Chem. Soc.  1983,  105:  7672 
  • 2b Dneprovskii AS. Eliseenkov EV. Russ. J. Org. Chem.  1994,  30:  235 
  • 3a Sopwith W. Hart T. Garner P. BMC Infect. Dis.  2002,  2:  4 
  • 3b Rutala WA. Weber DJ. Clin. Microbiol. Rev.  1997,  10:  597 
  • 4 U.S. Army Medical Research Institute of Medical Defense USAMRICD’s Medical Management of Chemical Casualties Handbook   3rd ed.: International Medical Publishing Inc., McLean; VA (USA): 2002. 
  • 5 Sugam R. Helz GR. Environ. Sci. Technol.  1976,  10:  384 
  • 6a Gilliotte BJ. Sanders CL. Wall LK. Landolt RG. J. Org. Chem.  1986,  51:  3233 
  • 6b Landolt RG. Fuel  1975,  54:  299 
  • 6c Angert JL. Gatton SL. Reilly MT. Landolt RG. Fuel  1977,  56:  224 
  • 6d Landolt RG. Davis GM. Reilly MT. Reinhold DS. Landolt RGD. Chem. Ind. (London, U.K.)  1980,  292 
  • 6e Elmore PR. Reed RT. Terkle-Husllig T. Welch JS. Young SM. J. Org. Chem.  1989,  54:  970 
  • 6f O’Connor KJ. Burrows CJ. J. Org. Chem.  1991,  56:  1344 
  • 6g Arnold JT. Bayraktaroglu TO. Brown RG. Heiermann CR. Magnus WW. Ohman AB. Landolt RG. J. Org. Chem.  1992,  57:  391 
  • 6h Bayraktaroglu TO. Gooding MA. Khatib SF. Lee H. Kourouma M. Landolt RG. J. Org. Chem.  1993,  58:  1264 
  • 6i Hays RS. Hobbs GP. Kourouma M. Ries JJ. Ste Marie TM. Sherwood SKM. Landolt RG. J. Mol. Catal A: Chem.  1998,  L123 
  • 6j Dailey JI. Hays RS. Lee H. Mitchell RM. Ries JJ. Landolt RG. Husmann HH. Lockridge JB. Hendrickson WH. J. Org. Chem.  2000,  65:  2568 
  • 6k Bright ZR. Luyeye CR. Morton ASteM. Sedenko M. Landolt RG. Bronzi MJ. Bohovic KM. Gonser MWA. Lapainis TE. Hendrickson WH. J. Org. Chem.  2005,  70:  684 
  • 7 Cary FA. In Organic Chemistry   6th ed.:  McGraw-Hill; New York: 2005.  p.801-804  
  • 8 Personal communication with authors of ‘The Haloform Reaction in the Presence of Cyclodextrins’: Trotta F. Coantamessa D. Zanetti M. J. Inclusion Phenom. Macrocyclic Chem.  2000,  37:  83 
  • 9 Gonsalvi L. Arends I. Moilanen P. Sheldon R. Adv. Synth. Catal.  2003,  345:  1321 
  • 10 Dijksman A. Arends I. Sheldon R. Chem. Commun.  2000,  271 
  • 11 Xie H. Shang S. Duan H. Tetrahedron Lett.  2004,  45:  2013 
  • Overview of the ipso reactions:
  • 12a Aromatic Chemistry   Hepworth JD. Waring DR. Waring MJ. RSC; London: 2003.  p.34-38  
  • Analogous halodehydroxymethylations:
  • 12b Bravo A. Fontana F. Dordi B. Minisci F. J. Org. Chem.  2000,  65:  3880 
  • 12c Lee CK. Koo B.-S. Lee YS. Cho HK. Lee K.-J. Bull. Korean Chem. Soc.  2002,  23:  1667 
  • 12d Miller RA. Hoerrner RS. Org. Lett.  2003,  5:  285 
  • 14 Bradley L. Lesica J. Albertson K. React. Kinet. Catal. Lett.  1997,  62:  3 
  • 15 Spencer D. Henshall T. J. Am. Chem. Soc.  1955,  77:  1943 ; product isolated was identical to authentic material by mixed mp
  • 16a Abramovici A. Neuman R. Sasson Y. J. Mol. Catal.  1985,  29:  291 
  • See also:
  • 16b Abramovici A. Neuman R. Sasson Y. J. Mol. Catal.  1985,  29:  299 
  • 17 Walling C. McGuinness JA. J. Am. Chem. Soc.  1969,  91:  2053 ; and references cited therein
  • 18a

    A reviewer has suggested that a free-radical chain mechanism can be considered as a plausible alternative to electrophilic aromatic substitution.

  • 18b Groups, whether they activate or deactivate other ring positions, may be replaced by ipso-electrophilic substitution. See: Traynham JG. J. Chem. Educ.  1983,  60:  937 ; and references cited therein
13

Carrillo, H.; Rodriguez, A.; Melendez, J.; Oropeza, M.; Ngo, M.; Woods, G.; Landolt, R. G. Hypochlorite-Induced IPSO Reactions of an Aromatic Alcohol; Poster 215, 64th Southwest Regional ACS Meeting, Little Rock, AR. 2008 (accessed August 2010), http://acs.confex.com/acs/swrm08/techprogram/P60964.HTM, accessed December, 2010.