Synlett 2005(17): 2619-2622  
DOI: 10.1055/s-2005-917102
LETTER
© Georg Thieme Verlag Stuttgart · New York

[5+1] Cocyclization of (Cyclopropylmethylene)cyclopropanes and other Vinylcyclopropanes with Carbon Monoxide Catalyzed by Octacarbonyldicobalt [1]

Takuya Kurahashi, Armin de Meijere*
Institut für Organische und Biomolekulare Chemie der Georg-August-Universität Göttingen, Tammannstrasse 2, 37077 Göttingen, Germany
Fax: +49(551)399475; e-Mail: Armin.deMeijere@chemie.uni-goettingen.de;
Further Information

Publication History

Received 25 July 2005
Publication Date:
05 October 2005 (online)

Abstract

Vinylcyclopropanes react with octacarbonyldicobalt ­stoichiometrically under mild conditions to give cyclohex-3-enones in moderate to good yields (51-75%). Catalytic amounts of the cobalt­carbonyl complex or a rhodiumcarbonyl complex also ­mediate [5+1] cocyclizations of vinylcyclopropanes with carbon monoxide (under CO balloon pressure) to give cyclohex-3-enones in good yields (up to 95%).

    References

  • 1a Part 120 in the series ‘Cyclopropyl Building Blocks for Organic Synthesis’. For Part 119 see: Dalai S. Limbach M. Zhao L. Tamm M. Sevvana M. de Meijere A. Synthesis  2005,  in press 
  • 1b For Part 118 see: Yucel B. Arve L. de Meijere A. Tetrahedron  2005,  in press 
  • 2 Oppolzer W. In Comprehensive Organic Synthesis   Vol. 5:  Trost BM. Fleming I. Paquette LA. Pergamon; Oxford: 1991.  p.315 
  • 3 For a comprehensive review on the stoichiometric Pauson-Khand reaction see: Schore NE. In Comprehensive Organic Synthesis   Vol. 5:  Trost BM. Fleming I. Paquette LA. Pergamon; Oxford: 1991.  p.1037 
  • For recent reviews on the Pauson-Khand reaction see:
  • 4a Blanco-Urgoiti J. Anorbe L. Perez-Serrano L. Dominguez G. Perez-Castells J. Chem. Soc. Rev.  2004,  33:  32 
  • 4b Gibson SE. Stevenazzi A. Angew. Chem. Int. Ed.  2003,  42:  1800 ; Angew. Chem. 2003, 115, 1844
  • 4c Rivero MR. Adrio J. Carretero JC. Eur. J. Org. Chem.  2002,  2881 
  • 4d Brummond KM. Kent JL. Tetrahedron  2000,  56:  3263 
  • [5+1] Cocyclizations of vinylcyclopropanes:
  • 5a Ben-Shoshan R. Sarel S. J. Chem. Soc., Chem. Commun.  1969,  883 
  • 5b Victor R. Ben-Shoshan R. Sarel S. Tetrahedron Lett.  1970,  11:  4253 
  • 5c Sarel S. Acc. Chem. Res.  1978,  11:  204 
  • 5d Aumann R. J. Am. Chem. Soc.  1974,  96:  2631 
  • 5e Taber DF. Kanai K. Jiang Q. Bui G. J. Am. Chem. Soc.  2000,  122:  6807 
  • 5f Taber DF. Joshi PV. Kanai K. J. Org. Chem.  2004,  69:  2268 
  • [5+1] Cocyclizations with cyclopropene derivatives:
  • 5g Grabowski NA. Hughes RP. Jaynes BS. Rheingold AL. J. Chem. Soc., Chem. Commun.  1986,  1694 
  • 5h Cho SH. Liebeskind LS. J. Org. Chem.  1987,  52:  2631 
  • 5i Semmelhack MF. Ho S. Steigerwald M. Lee MC. J. Am. Chem. Soc.  1987,  109:  4397 
  • [5+1] Cocyclizations of allenylcyclopropanes:
  • 5j Iwasawa N. Owada Y. Matsuo T. Chem. Lett.  1995,  115 
  • 5k Owada Y. Matsuo T. Iwasawa N. Tetrahedron  1997,  53:  11069 
  • Iridium-catalyzed [5+1] cycloadditions of allenylcyclopropanes:
  • 5l Murakami M. Itami K. Ubukata M. Tsuji I. Ito Y. J. Org. Chem.  1998,  63:  4 
  • Ruthenium-catalyzed [5+1] cocyclizations of cyclopropyl ketimines:
  • 5m Kamitani A. Chatani N. Morimoto T. Murai S. J. Org. Chem.  2000,  65:  9230 
  • 6 Wiberg KB. Ellison GB. Wendoloski JJ. Brundle CR. Kuebler NA. J. Am. Chem. Soc.  1976,  98:  7179 
  • 7a Carbocyclic Three-Membered Ring Compounds, In Methods of Organic Chemistry (Houben-Weyl)   Vol. E17a-c:  de Meijere A. Thieme; Stuttgart: 1996. 
  • 7b Brandi A. Goti A. Chem. Rev.  1998,  98:  589 
  • 8 For a stable methylenecyclopropanecobalt complex see: Förster J. Kozhushkov SI. Binger P. Wedemann P. Noltemeyer M. de Meijere A. Butenschön H. Chem. Commun.  1998,  239 
  • 9 For cobalt-mediated Pauson-Khand reactions involving methylenecyclopropanes see: de Meijere A. Becker H. Stolle A. Kozhushkov SI. Bes MT. Salaün J. Noltemeyer M. Chem. Eur. J.  2005,  11:  2471 ; and references cited therein
  • 10 A cobalt complex-catalyzed [3+1] cocyclization of CO and methylenecyclopropanes without a vinyl substituent involving a cobaltacyclopropane intermediate has also been observed. See: Kurahashi T. de Meijere A. Angew. Chem. Int. Ed.  2005,  in press 
  • For cyclopropylmethylmetal to homoallylmetal rearrangements concerning other transition metals see:
  • 11a de Meijere A. Nüske H. Es-Sayed M. Labahn T. Schroen M. Bräse S. Angew. Chem. Int. Ed.  1999,  38:  3669 ; Angew. Chem. 1999, 111, 3881
  • 11b Nüske H. Noltemeyer M. de Meijere A. Angew. Chem. Int. Ed.  2001,  40:  3411 ; Angew. Chem. 2001, 113, 3509
  • 11c Larock RC. Varaprath S. J. Org. Chem.  1984,  49:  3432 
  • 11d Trost BM. Toste FD. Shen H. J. Am. Chem. Soc.  2000,  122:  2379 
  • 11e Wender PA. Williams TJ. Angew. Chem. Int. Ed.  2002,  41:  4550 ; Angew. Chem. 2002, 114, 4732
  • 11f Wender PA. Husfeld CO. Langkopf E. Love JA. Pleuss N. Tetrahedron  1998,  54:  7203 
  • 12a Khand IU. Knox GR. Pauson PL. Watts WE. Foreman MI. J. Chem. Soc., Perkin Trans. 1  1973,  977 
  • 12b Billington DC. Kerr WJ. Pauson PL. Farnocchi CF. J. Organomet. Chem.  1988,  356:  213 
  • 12c Rautenstrauch V. Mégard P. Conesa J. Küster W. Angew. Chem., Int. Ed. Engl.  1990,  29:  1413 ; Angew. Chem. 1990, 102, 1441
  • 12d Jeong N. Hwang SH. Lee YS. Chung YK. J. Am. Chem. Soc.  1994,  116:  3159 
  • 12e Lee BY. Chung YK. Jeong N. Lee YS. Hwang SH. J. Am. Chem. Soc.  1994,  116:  8793 
  • 12f Jeong N. Hwang SH. Lee YW. Lim JS. J. Am. Chem. Soc.  1997,  119:  10549 
  • 12g Pagenkopf BL. Livinghouse T. J. Am. Chem. Soc.  1996,  118:  2285 
13

Representative Procedure.
To a solution of octacarbonyldicobalt (17 mg, 0.05 mmol) in THF (10 mL) was added vinylcyclopropane 1a (108 mg, 1 mmol), and the mixture was heated at 60 °C for 12 h under an atmosphere of CO provided in a balloon. The cooled reaction mixture was diluted with Et2O (20 mL) and stirred under air for 1 h. Filtration through a pad of Celite and purification by Kugelrohr distillation gave 2a (92 mg, 0.68 mmol, 68%) as a pale yellow oil. R f = 0.22 (hexane-Et2O 10:1). 1H NMR (500 MHz, CDCl3): δ = 1.11 (dd, J = 7.4, 4.0 Hz, 2 H), 1.35 (dd, J = 7.4, 4.0 Hz, 2 H), 1.47 (m, 3 H), 2.38 (m, 2 H), 2.49 (m, 2 H), 5.72 (m, 1 H). 13C NMR (125 MHz, CDCl3): δ = 16.2 (cPr-C), 17.6 (CH3), 22.5 (CH2), 31.9 (C), 38.5 (CH2), 120.0 (CH), 133.8 (C), 210.7 (CO). IR (neat): 3002, 2965, 2922, 2854, 1701, 1437, 1414, 1354, 1182, 1115, 1031, 950, 848, 668 cm-1. MS: m/z = 137/136/135 (10/100/48) [M+], 121 (62) [M+ - Me], 185 (10), 93 (61), 79 (50), 77 (44). Anal. Calcd for C9H12O (136.2): C, 79.37; H, 8.88. Found: C, 79.22; H, 8.76.