Synthesis 2012; 44(9): 1349-1352
DOI: 10.1055/s-0031-1290753
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of a New Chiral Sulfonic Acid

Joydeb Das
Laboratoire de Chimie Moléculaire et Thio-organique, ENSICAEN, Université de Caen, UMR CNRS 6507, INC3M FR 3038, 6 boulevard du Maréchal Juin, 14050 Caen, France, Fax: +33(2)31452877   Email: jerome.blanchet@ensicaen.fr
,
Fabien Le Cavelier
Laboratoire de Chimie Moléculaire et Thio-organique, ENSICAEN, Université de Caen, UMR CNRS 6507, INC3M FR 3038, 6 boulevard du Maréchal Juin, 14050 Caen, France, Fax: +33(2)31452877   Email: jerome.blanchet@ensicaen.fr
,
Jacques Rouden
Laboratoire de Chimie Moléculaire et Thio-organique, ENSICAEN, Université de Caen, UMR CNRS 6507, INC3M FR 3038, 6 boulevard du Maréchal Juin, 14050 Caen, France, Fax: +33(2)31452877   Email: jerome.blanchet@ensicaen.fr
,
Jérôme Blanchet*
Laboratoire de Chimie Moléculaire et Thio-organique, ENSICAEN, Université de Caen, UMR CNRS 6507, INC3M FR 3038, 6 boulevard du Maréchal Juin, 14050 Caen, France, Fax: +33(2)31452877   Email: jerome.blanchet@ensicaen.fr
› Author Affiliations
Further Information

Publication History

Received: 12 January 2012

Accepted after revision: 17 February 2012

Publication Date:
28 March 2012 (online)


Abstract

A convenient route to an original chiral sulfonic acid is disclosed. The synthesis is based on an optimized and regioselective direct bis-orthoarylation of a commercially available phenol, followed by a Newman–Kwart rearrangement. Resolution by preparative chiral HPLC and oxidative cleavage give the targeted Brønsted acid in >99% ee.

 
  • References

    • 1a Terada M. Synthesis 2010; 1929
    • 1b Kampen D, Resinger CM, List B. Top. Curr. Chem. 2010; 291: 395
    • 1c Schenker S, Zamfir A, Freund M, Tsogoeva SB. Eur. J. Org. Chem. 2011; 2209
    • 1d Akiyama T, Itoh J, Fuchibe K. Adv. Synth. Catal. 2006; 348: 999
  • 2 Rueping M, Nachtsheim BJ, Ieawsuwan W, Atodiresei I. Angew. Chem. Int. Ed. 2011; 50: 6706
    • 3a For the substitution of oxygen atoms with sulfur or selenium, see: Cheon CH, Yamamoto H. J. Am. Chem. Soc. 2008; 130: 9246
    • 3b For the specific phosphorodithioic acids, see: Pousse G, Devineau A, Dalla V, Humphreys L, Lasne M.-C, Rouden J, Blanchet J. Tetrahedron 2009; 65: 10617
    • 3c See also: Shapiro ND, Rauniyar V, Hamilton GL, Wu J, Toste FD. Nature 2011; 470: 245
    • 4a García-García P, Lay F, García-García P, Rabalakos C, List B. Angew. Chem. Int. Ed. 2009; 48: 4363
    • 4b List B, Classen G, Ladepeche A, Kampen D. Adv. Synth. Catal. 2008; 350: 962
    • 4c Pan SC, List B. Chem.–Asian J. 2008; 3: 430
  • 5 Susperregui N, Delcroix D, Martin-Vaca B, Bourissou D, Maron L. J. Org. Chem. 2010; 75: 6581
    • 6a Saito S, Hatanaka K, Kano T, Yamamoto H. Angew. Chem. Int. Ed. 1998; 37: 3378
    • 6b Saito S, Kano T, Hatanaka K, Yamamoto H. J. Org. Chem. 1997; 62: 5651
    • 6c Saito S, Kano T, Hatanaka K, Yamamoto H. Org. Lett. 2000; 2: 1891
  • 8 Saito S, Kano T, Muto H, Nakadai M, Yamamoto H. J. Am. Chem. Soc. 1999; 121: 8943
    • 9a Barton DH. R, Donnelly DM. X, Guiry PJ, Reibenspies JH. J. Chem. Soc., Chem. Commun. 1990; 1110
    • 9b Akland DJ, Pinhey JT. J. Chem. Soc., Perkin Trans. 1 1987; 2695
    • 9c Morgan J, Pinhey JT. J. Chem. Soc., Perkin Trans. 1 1990; 715
  • 10 Gilday JP, Lenden P, Moseley JD, Cox BG. J. Org. Chem. 2008; 73: 3130
  • 11 Harvey JN, Jover J, Lloyd-Jones GC, Moseley JD, Murray P, Renney JS. Angew. Chem. Int. Ed. 2009; 48: 7612
  • 12 Armet O, Veciana J, Castaner J, Riera J, Carilla J. Phosphorus Sulfur Relat. Elem. 1988; 35: 273
  • 13 The separation of racemic sulfonic acid 2 on an analytical scale was possible (Daicel Chiralpak® QN-AX, MeOH–AcOH/NH4OAc (98:1.5:0.5, 25 °C, 1 mL/min), but cost-prohibitive on a semi-preparative scale