Synlett 2010(19): 2947-2949  
DOI: 10.1055/s-0030-1259031
LETTER
© Georg Thieme Verlag Stuttgart ˙ New York

Regioselective Alkylation of Catechols via Mitsunobu Reactions

Xiaolong Wang*a, Tingting Jua, Xiaodong Lia, Xiaoping Caob
a School of Chemical and Biological Engineering, Lanzhou Jiaotong University, Lanzhou 730070, P. R. of China
Fax: +86(931)4956512; e-Mail: wangxl@mail.lzjtu.cn;
b Department of Chemistry, State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, P. R. of China
Further Information

Publication History

Received 1 September 2010
Publication Date:
10 November 2010 (online)

Abstract

A mild and efficient Mitsunobu protocol for the regioselective alkylation of catechols such as 3,4-dihydroxybenzaldehyde and methyl 3,4-dihydroxybenzoate is described. The para-alkylation products could be easily prepared via the Mitsunobu reaction with high selectivity in moderate to good yields.

    References and Notes

  • 1a Gu W.-X. Jing X.-B. Pan X.-F. Chan ASC. Yang T.-K. Tetrahedron Lett.  2000,  41:  6079 
  • 1b Banwell MG. Chand S. Savage GP. Tetrahedron: Asymmetry  2005,  16:  1645 
  • 1c Reitz A. Avery MA. Verlander MS. Goodman M. J. Org. Chem.  1981,  46:  4859 
  • 1d Desroses M. Laconde G. Depredux P. Hénichart J.-P. Org. Prep. Proced. Int.  2004,  36:  445 
  • 1e Pederson AMP. Ward EM. Schoonover DV. Slebodnick C. Gibson HW.
    J. Org. Chem.  2008,  73:  9094 
  • 1f Meuzelaar GJ. van Vliet MCA. Maat L. Sheldon RA. Eur. J. Org. Chem.  1999,  2315 
  • 2a Wymann WE. Davis R. Patterson JW. Pfister JR. Synth. Commun.  1988,  18:  1379 
  • 2b Kessar SV. Gupta YP. Mohammad T. Goyal M. Sawal KK.
    J. Chem. Soc., Chem. Commun.  1983,  400 
  • 2c Hegedüs B. Helv. Chim. Acta  1963,  2604 
  • 2d Hänsel R. Su T.-L. Schulz J. Chem. Ber.  1977,  110:  3664 
  • 2e Plourde GL. Spaetzel RR. Molecules  2002,  7:  697 
  • 2f He C.-L. Shi Z.-M. Zhou Q.-Z. Li S.-J. Li N. Huang F.-H. J. Org. Chem.  2008,  73:  5872 
  • 2g Orchard MG, Neuss JC, and Galley CMS. inventors; Patent US  7105554B2. 
  • 3a Mitsunobu O. Synthesis  1981,  1 
  • 3b Nune SK. Synlett  2003,  1221 
  • 3c Kumara Swamy KC. Bhuvan Kumar NN. Balaraman E. Pavan Kumar KVP. Chem. Rev.  2009,  109:  2551 
  • 4a Manivel P. Rai NP. Jayashankara VP. Arunachalam PN. Tetrahedron Lett.  2007,  48:  2701 
  • 4b Caras-Quintero D. Bäuerle P. Chem. Commun.  2002,  2690 
  • 4c Cao X.-P. Tetrahedron  2002,  58:  1301 
  • 4d Cao X.-P. Chan T.-L. Chow H.-F. Tu J. J. Chem. Soc., Chem. Commun.  1995,  1297 
  • 4e Brosse N. Pinto MF. Bodiguel J. Jamart-Grégoire B. J. Org. Chem.  2001,  66:  2869 
  • 4f Holub N. Neidhöfer J. Blechert S. Org. Lett.  2005,  7:  1227 
  • 4g Hillier MC. Desrosiers JN. Marcoux JE. Grabowski EJJ. Org. Lett.  2004,  6:  573 
  • 4h Anderson NG. Lust DA. Colapret KA. Simpson JH. Malley MF. Gougoutas JZ. J. Org. Chem.  1996,  61:  7955 
  • 5a Gu W.-X. Chen X.-C. Pan X.-F. Chan ASC. Yang T.-K. Tetrahedron: Asymmetry  2000,  11:  2801 
  • 5b Kummeter M. Kazmaier U. Eur. J. Org. Chem.  2003,  3330 
  • 5c Tron GC. Pagliai F. Grosso ED. Genazzani AA. Sorba G. J. Med. Chem.  2005,  48:  3260 
  • 5d Shimokawa J. Shirai K. Tanatani A. Hashimoto Y. Nagasawa K. Angew. Chem. Int. Ed.  2004,  43:  1559 
  • 5e Shen R. Lin CT. Porco JA. J. Am. Chem. Soc.  2002,  124:  5650 
  • 6a Pautard-Cooper A. Evans SA. J. Org. Chem.  1988,  53:  2300 
  • 6b Pautard-Cooper A. Evans SA. J. Org. Chem.  1989,  54:  2485 
  • 6c Saeed M. Ilg T. Schick M. Abbas M. Voelter W. Tetrahedron Lett.  2001,  42:  7401 
  • 6d Wang F.-D. Yue J.-M. Eur. J. Org. Chem.  2005,  2575 
  • 7 Wang G.-J. Ella-Menye J.-R. Martin MS. Yang H. Williams K. Org. Lett.  2008,  10:  4203 
  • 8 Tahir H. Hindsgaul O. J. Org. Chem.  2000,  65:  911 
  • 9 Ko SY. J. Org. Chem.  2002,  67:  2689 
  • 10 Ang K.-P. Tan S.-F. J. Chem. Soc., Perkin Trans. 2  1979,  1525 
  • 11a Wang X.-L. Liu D. Xia Y.-M. Cao X.-P. Pan X.-F. Chin. J. Chem.  2004,  22:  467 
  • 11b Ding T. Wang X. Cao X. Chin. J. Chem.  2006,  24:  1618 
  • 12 Wang X.-L. Li X.-D. Xue J.-J. Zhao Y.-L. Zhang Y.-M. Tetrahedron Lett.  2009,  50:  413 
  • 13a Kim Y.-W. Hackett JC. Brueggemeier RW. J. Med. Chem.  2004,  47:  4032 
  • 13b Pettus LH. Van De Water RW. Pettus TRR. Org. Lett.  2001,  3:  905 
  • 13c Kim Y.-W. Mobley JA. Brueggemeier RW. Bioorg. Med. Chem. Lett.  2003,  13:  1475 
14

General Procedure for the Regioselective Alkylation under Mitsunobu Conditions: DIAD (4.5 mmol) and Ph3P (4.5 mmol) were dissolved in anhyd THF (20 mL), and the solution was cooled in an ice bath. Alcohol (3 mmol) was added. After the mixture was stirred for 10 min, a solution of catechol (3 mmol) in anhyd THF (5 mL) was added immediately. After stirring for 30 min, the reaction mixture was warmed to r.t. and stirred. When the reaction was judged to be complete (TLC), the mixture was evaporated under vacuum and the residue was purified by column chroma-tography on silica gel eluting with a mixture of PE and EtOAc.
Spectral Data for Methyl 4-Butyloxy-3-hydroxybenzoate (Table 1, Entry 10): colorless crystals; mp 114-115 ˚C. ¹H NMR (400 MHz, CDCl3): δ = 0.99 (t, J = 7.2 Hz, 3 H), 1.50 (m, 2 H), 1.82 (m, 2 H), 3.87 (s, 3 H), 4.10 (t, J = 6.4 Hz, 2 H), 5.71 (s, 1 H), 6.85 (d, J = 9.2 Hz, 1 H), 7.59 (m, 2 H). ¹³C NMR (100 MHz, CDCl3): δ = 13.7, 19.1, 31.0, 51.9, 68.8, 110.6, 115.5, 122.7, 123.1, 145.3, 149.8, 166.8.