Synthesis 2015; 47(19): 2912-2923
DOI: 10.1055/s-0035-1560457
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© Georg Thieme Verlag Stuttgart · New York

Palladium-Catalyzed Heck-Type Difluoroalkylation of Alkenes with Functionalized Difluoromethyl Bromides

Feng Zhang
Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, P. R. of China   Email: xgzhang@mail.sioc.ac.cn
,
Qiao-Qiao Min
Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, P. R. of China   Email: xgzhang@mail.sioc.ac.cn
,
Xingang Zhang*
Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, P. R. of China   Email: xgzhang@mail.sioc.ac.cn
› Author Affiliations
Further Information

Publication History

Received: 02 July 2015

Accepted after revision: 27 July 2015

Publication Date:
17 August 2015 (online)


Abstract

An efficient method for the synthesis of difluoroalkylated alkenes through palladium-catalyzed Heck-type reaction with functionalized difluoromethyl bromides has been developed. The advantages of this protocol are its synthetic simplicity, excellent functional group compatibility, and efficient late-stage difluoroalkylation of biologically relevant molecules, thus paving a new way for application in drug discovery and development. Mechanistic studies revealed that the free difluoroalkyl radicals, initiated by a [Pd(0)Ln] via a single-electron-transfer (SET) pathway, were involved in the Heck-type catalytic cycle.

Supporting Information

 
  • References

    • 1a Modern Carbonyl Olefination . Takeda T. Wiley-VCH; Weinheim: 2004
    • 1b Takahashi A, Kirio Y, Sodeoka M, Sasai H, Shibasaki M. J. Am. Chem. Soc. 1989; 111: 643
    • 1c Wu X-F, Fang X, Wu L, Jackstell R, Neumann N, Beller M. Acc. Chem. Res. 2014;  47:  1041
    • 2a Smart BE. J. Fluorine Chem. 2001; 109: 3
    • 2b Müller K, Faeh C, Diederich F. Science 2007; 317: 1881
    • 2c O’Hagan D. Chem. Soc. Rev. 2008; 37: 308
    • 2d Purser S, Moore PR, Swallow S, Gouverneur V. Chem. Soc. Rev. 2008; 37: 320

      For selected reviews, see:
    • 3a Furuya T, Kamlet AS, Ritter T. Nature 2011; 473: 470
    • 3b Tomashenko OA, Grushin VV. Chem. Rev. 2011; 111: 4475
    • 3c Hollingworth C, Gouverneur V. Chem. Commun. 2012; 48: 2929
    • 3d Besset T, Schneider C, Cahard D. Angew. Chem. Int. Ed. 2012; 51: 5048
    • 3e Qing F.-L. Chin. J. Org. Chem. 2012; 32: 815
    • 3f Ni C, Zhu L, Hu J. Acta Chim. Sinica 2015; 73: 90
    • 3g Belhomme M.-C, Besset T, Poisson T, Pannecoucke X. Chem. Eur. J. 2015; 21 in press; DOI: 10.1002/chem.201501475
  • 4 Besset T, Poisson T, Pannecoucke X. Chem. Eur. J. 2014; 20: 16830
  • 5 Taguchi T, Kitagawa O, Morikawa T, Nishiwaki T, Uehara H, Endo H, Kobayashi Y. Tetrahedron Lett. 1986; 27: 6103
  • 6 Yokomatsu T, Suemune K, Murano T, Shibuya S. J. Org. Chem. 1996; 61: 7207
    • 7a Fier PS, Hartwig JF. J. Am. Chem. Soc. 2012; 134: 5524
    • 7b Prakash GK. S, Ganesh SK, Jones J.-P, Kulkarni A, Masood K, Swabeck JK, Olah GA. Angew. Chem. Int. Ed. 2012; 51: 12090
  • 8 Schwaebe MK, McCarthy JR, Whitten JP. Tetrahedron Lett. 2000; 41: 791
    • 9a Long Z.-Y, Chen Q.-Y. J. Org. Chem. 1999; 64: 4775
    • 9b Murakami S, Ishii H, Fuchigami T. J. Fluorine Chem. 2004; 125: 609
    • 9c Ghattas W, Hess CR, Iacazio G, Hardre R, Klinman JP, Reglier M. J. Org. Chem. 2006; 71: 8618
    • 9d Yu C, Iqbal N, Park S, Cho EJ. Chem. Commun. 2014; 50: 12884

      For selected examples, see:
    • 10a Affo W, Ohmiya H, Fujoka T, Ikeda Y, Nakamura T, Yorimitsu H, Oshima K, Imamura Y, Mizuta T, Miyoshi K. J. Am. Chem. Soc. 2006; 128: 8068
    • 10b Firmansjah L, Fu GC. J. Am. Chem. Soc. 2007; 129: 11340
    • 10c Standley EA, Jamison TF. J. Am. Chem. Soc. 2013; 135: 1585
    • 10d Matsubara R, Gutierrez AC, Jamison TF. J. Am. Chem. Soc. 2011; 133: 19020
    • 10e Bloome KS, McMahen RL, Alexanian EJ. J. Am. Chem. Soc. 2011; 133: 20146
    • 10f Zhou Y, Zhou JS. Chem. Commun. 2014; 50: 3725
  • 11 Surapanich N, Kuhakarn C, Pohmakotr M, Reutrakul V. Eur. J. Org. Chem. 2012; 5943
  • 12 Feng Z, Min Q.-Q, Zhao H.-Y, Gu J.-W, Zhang X. Angew. Chem. Int. Ed. 2015; 54: 1270

    • A copper-catalyzed difluoroacetylation of dihydropyrans and enamides has also been reported recently. However, the styrene derivatives were not suitable substrates, see:
    • 13a Belhomme M.-C, Poisson T, Pannecoucke X. Org. Lett. 2013; 15: 3428
    • 13b Caillot G, Dufour J, Belhomme M.-C, Poisson T, Grimaud L, Pannecoucke X, Gillaizeau I. Chem. Commun. 2014; 50: 5887

      For our contribution in transition-metal-catalyzed difluoroalkylation reactions, see:
    • 14a Feng Z, Chen F, Zhang X. Org. Lett. 2012; 14: 1938
    • 14b Feng Z, Min Q.-Q, Xiao Y.-L, Zhang B, Zhang X. Angew. Chem. Int. Ed. 2014; 53: 1669
    • 14c Min Q.-Q, Yin Z, Guo W.-H, Zhang X. J. Am. Chem. Soc. 2014; 136: 1230
    • 14d Xiao Y.-L, Guo W.-H, He G.-Z, Pan Q, Zhang X. Angew. Chem. Int. Ed. 2014; 53: 9909
    • 14e Yu Y.-B, He G.-Z, Zhang X. Angew. Chem. Int. Ed. 2014; 53: 10457
    • 14f Xiao Y.-L, Zhang B, Feng Z, Zhang X. Org. Lett. 2014; 16: 4822
    • 14g Feng Z, Xiao Y.-L, Zhang X. Org. Chem. Front. 2014; 1: 113
    • 14h Gu J.-W, Guo W.-H, Zhang X. Org. Chem. Front. 2015; 2: 38

      For a study on the reductive elimination from [ArPd(Xantphos)CF3] complex, see:
    • 15a Grushin VV, Marshall WJ. J. Am. Chem. Soc. 2006; 128: 12644
    • 15b Bakhmutov VI, Bozoglian F, Gómez K, González G, Grushin VV, Macgregor SA, Martin E, Miloserdov FM, Novikov MA, Panetier JA, Romasho LV. Organometallics 2012; 31: 1315
    • 16a Patil PO, Bari SB, Firke SD, Deshmukh PK, Donda ST. Bioorg. Med. Chem. 2013; 21: 2434
    • 16b Poulie CB. M, Bunch L. ChemMedChem 2013; 8: 205
    • 16c Dickinson JM. Nat. Prod. Rep. 1993; 10: 71
    • 17a Wegert A, Miethchen R, Hein M, Reinke H. Synthesis 2005; 1850
    • 17b Leclerc E, Pannecoucke X, Etheve-Quelquejeu M, Sollogoub M. Chem. Soc. Rev. 2013; 42: 4270
    • 18a Smits R, Koksch B. Curr. Top. Med. Chem. 2006; 6: 1483
    • 18b Fustero S, Sanz-Cervera JF, Acena JL, Sanchez-Rosello M. Synlett 2009; 525
  • 19 Huang X.-T, Chen Q.-Y. J. Org. Chem. 2001; 66: 4651

    • For radical clock experiments using α-cyclopropylstyrene, see:
    • 20a Baldwin JE. Chem. Rev. 2003; 103: 1197
    • 20b Shirakawa E, Zhang X, Hayashi T. Angew. Chem. Int. Ed. 2011; 50: 4671
    • 20c Liwosz TW, Chemler SR. Org. Lett. 2013; 15: 3034
    • 21a For a pioneering study of Pd-initiated fluoroalkyl radical from perfluoroalkyl iodides, see: Chen Q.-Y, Yang Z.-Y, Zhao C.-X, Qiu Z.-M. J. Chem. Soc., Perkin Trans. 1 1988; 563
    • 21b This paper has also demonstrated that it is difficult for RfPdI(PPh3)2 complex to react with alkenes