Synthesis 2022; 54(24): 5520-5528
DOI: 10.1055/a-1918-4406
paper

N-Heterocyclic Carbene Catalyzed Cross Dehydrogenative Coupling of Aldehydes with Methanol: Combined Use of Eosin Y and Hexachloroethane

Eito Yoshioka
,
Hiroki Takahashi
,
Akane Kubo
,
Miki Ohno
,
Fuuka Watanabe
,
Rino Shiono
,
Yuuki Miyazaki
,
Hideto Miyabe
This work was supported by a Japan Society for the Promotion of Science­ (JSPS) KAKENHI Grant-in-Aid for Scientific Research (C) (Grant Number 20K06954, to H.M.).


Abstract

Cross dehydrogenative coupling of aldehydes with methanol was investigated under organocatalytic conditions based on the cooperation­ between N-heterocyclic carbene and eosin Y·Na as an organophotocatalys­t. The combined use of eosin Y·Na and hexachloro­ethane (C2Cl6) was the effective method for the oxidative esterification of various aldehydes, because the oxidation steps are promoted by two pathways associated with the activated photocatalyst and C2Cl6. In contrast, the combined use of eosin Y·Na and bromotrichloromethane (BrCCl3) was effective only for the oxidative esterification of simple cinnamaldehyde derivatives, in which BrCCl3 promotes the oxidation as a brominating reagent toward radical intermediates.

Supporting Information



Publication History

Received: 01 July 2022

Accepted: 04 August 2022

Accepted Manuscript online:
04 August 2022

Article published online:
14 September 2022

© 2022. Thieme. All rights reserved

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References


    • For reviews, see:
    • 1a Liu C, Yuan J, Gao M, Tang S, Li W, Shi R, Lei A. Chem. Rev. 2015; 115: 12138
    • 1b Gini A, Brandhofer T, Mancheño OG. Org. Biomol. Chem. 2017; 15: 1294
    • 1c Yang Y, Lan J, You J. Chem. Rev. 2017; 117: 8787
    • 1d Wang H, Gao X, Lv Z, Abdelilah T, Lei A. Chem. Rev. 2019; 119: 6769
    • 1e Bagdi AK, Rahman M, Bhattacherjee D, Zyryanov GV, Ghosh S, Chupakhin ON, Hajra A. Green Chem. 2020; 22: 6632
    • 1f Yuan Y, Yang J, Lei A. Chem. Soc. Rev. 2021; 50: 10058

      For reviews, see:
    • 2a Krylov IB, Vil’ VA, Terent’ev AO. Beilstein J. Org. Chem. 2015; 11: 92
    • 2b Borpatra PJ, Deka B, Deb ML, Baruah PK. Org. Chem. Front. 2019; 6: 3445

      Selected examples, see:
    • 3a Travis BR, Sivakumar M, Hollist GO, Borhan B. Org. Lett. 2003; 5: 1031
    • 3b Schulze A, Giannis A. Adv. Synth. Catal. 2004; 346: 252
    • 3c Tank R, Pathak U, Vimal M, Bhattacharyya S, Pandey LK. Green Chem. 2011; 13: 3350
    • 3d Kuwano S, Harada S, Oriez R, Yamada K. Chem. Commun. 2012; 48: 145
    • 3e Mineno T, Sakai M, Ubukata A, Nakahara K, Yoshimitsu H, Kansui H. Chem. Pharm. Bull. 2013; 61: 870
    • 3f Feng J.-B, Gong J.-L, Li Q, Wu X.-F. Tetrahedron Lett. 2014; 55: 1657
    • 3g Lv Y, Sun K, Pu W, Mao S, Li G, Niu J, Chen Q, Wang T. RCS Adv. 2016; 6: 93486
    • 3h Xu X, Li P, Huang Y, Tong C, Yan Y, Xie Y. Tetrahedron Lett. 2017; 58: 1742
    • 4a Wei W, Zhang C, Xu Y, Wan X. Chem. Commun. 2011; 47: 10827
    • 4b Tan B, Toda N, Barbas CF. III. Angew. Chem. Int. Ed. 2012; 51: 12538
  • 5 Toledo H, Pisarevsky E, Abramovich A, Szpilman AM. Chem. Commun. 2013; 49: 4367
    • 6a Dinda M, Bose C, Ghosh T, Maity S. RCS Adv. 2015; 5: 44928
    • 6b Yi H, Hu X, Bian C, Lei A. ChemSusChem 2017; 10: 79

      Selected examples, see:
    • 7a Zhang J, Leitus G, Ben-David Y, Milstein D. J. Am. Chem. Soc. 2005; 127: 10840
    • 7b Yamamoto N, Obora Y, Ishii Y. J. Org. Chem. 2011; 76: 2937
    • 7c Gowrisankar S, Neumann H, Beller M. Angew. Chem. Int. Ed. 2011; 50: 5139
    • 7d Liu C, Tang S, Zheng L, Liu D, Zhang H, Lei A. Angew. Chem. Int. Ed. 2012; 51: 5662
    • 7e Zhang C, Jiao N. Org. Chem. Front. 2014; 1: 109
    • 7f Xu X, Sun J, Lin Y, Cheng J, Li P, Jiang X, Bai R, Xie Y. Eur. J. Org. Chem. 2017; 7160
    • 7g Zhu L, Ren X, Yu Y, Ou P, Wang Z.-X, Huang X. Org. Lett. 2020; 22: 2087

      For reviews, see:
    • 8a Enders D, Niemeier O, Henseler A. Chem. Rev. 2007; 107: 5606
    • 8b Flanigan DM, Romanov-Michailidis F, White NA, Rovis T. Chem. Rev. 2015; 115: 9307
    • 8c Wang MH, Scheidt KA. Angew. Chem. Int. Ed. 2016; 55: 14912
    • 8d Menon RS, Biju AT, Nair V. Beilstein J. Org. Chem. 2016; 12: 444
    • 8e Ren Q, Li M, Yuan L, Wang J. Org. Biomol. Chem. 2017; 15: 4731
    • 8f Chen X.-Y, Liu Q, Chauhan P, Enders D. Angew. Chem. Int. Ed. 2018; 57: 3862
    • 8g Miyabe H. Synthesis of Nitrogen-Heterocycles Based on N-Heterocyclic Carbene Organocatalysis. In More Synthetic Approaches to Nonaromatic Nitrogen Heterocycles, Vol. 1. Phillips AM. F. John Wiley & Sons; Hoboken: 2022: 163-212

      Selected examples for NHC-catalyzed oxidative esterification of aldehydes, see:
    • 9a Maki BE, Scheidt KA. Org. Lett. 2008; 10: 4331
    • 9b Noonan C, Baragwanath L, Connon SJ. Tetrahedron Lett. 2008; 49: 4003
    • 9c Sarkar S, Grimme S, Studer A. J. Am. Chem. Soc. 2010; 132: 1190
    • 9d Finney EE, Ogawa KA, Boydston AJ. J. Am. Chem. Soc. 2012; 134: 12374
    • 9e Delany EG, Fagan C.-L, Gundala S, Mari A, Broja T, Zeitler K, Connon SJ. Chem. Commun. 2013; 49: 6510
    • 9f White NA, Rovis T. J. Am. Chem. Soc. 2014; 136: 14674
    • 9g Chun S, Chung YK. Org. Lett. 2017; 19: 3787
    • 9h Wu Z, Jiang D, Wang J. Org. Chem. Front. 2019; 6: 688
    • 9i Liu Y, Majhi PK, Song R, Mou C, Hao L, Chai H, Jin Z, Chi YR. Angew. Chem. Int. Ed. 2020; 59: 3859
  • 10 DiRocco DA, Rovis T. J. Am. Chem. Soc. 2012; 134: 8094
    • 11a Yoshioka E, Inoue M, Nagoshi Y, Kobayashi A, Mizobuchi R, Kawashima A, Kohtani S, Miyabe H. J. Org. Chem. 2018; 83: 8962
    • 11b Yoshioka E, Takahashi H, Wanibe H, Hontani Y, Hatsuse K, Shimizu R, Kawashima A, Kohtani S, Miyabe H. Synthesis 2022; 54: 697
    • 12a Miyabe H. Recent Advances in Cooperative N-Heterocyclic Carbene Catalysis (Chap. 2). In Carbene. Saha S, Manna A. IntechOpen; London: 2022
    • 12b Dai L, Xia Z.-H, Gao Y.-Y, Gao Z.-H, Ye S. Angew. Chem. Int. Ed. 2019; 58: 18124
    • 12c Bay AV, Fitzpatrick KP, Betori RC, Scheidt KA. Angew. Chem. Int. Ed. 2020; 59: 9143
    • 12d Dai L, Ye S. Org. Lett. 2020; 22: 986
    • 12e Du D, Zhang K, Ma R, Chen L, Gao J, Lu T, Shi Z, Feng J. Org. Lett. 2020; 22: 6370
    • 12f Xia Z.-H, Dai L, Gao Z.-H, Ye S. Chem. Commun. 2020; 56: 1525
    • 12g Liu K, Studer A. J. Am. Chem. Soc. 2021; 143: 4903
  • 13 Wu X, Zhang Y, Wang Y, Ke J, Jeret M, Reddi RN, Yang S, Song B.-A, Chi YR. Angew. Chem. Int. Ed. 2017; 56: 2942
  • 14 Yan D.-M, Chen J.-R, Xiao W.-J. Angew. Chem. Int. Ed. 2019; 58: 378
  • 15 Sarkar SD, Biswas A, Samanta RC, Studer A. Chem. Eur. J. 2013; 19: 4664
    • 16a Kojima T, Obata R, Saito T, Einaga Y, Nishiyama S. Beilstein J. Org. Chem. 2015; 11: 200
    • 16b Chen X.-Y, Li S, Sheng H, Liu Q, Jafari E, von Essen C, Rissanen K, Enders D. Chem. Eur. J. 2017; 23: 13042
    • 16c Kise N, Iitaka S, Iwasaki K, Ueda N. J. Org. Chem. 2002; 67: 8305
    • 16d Kise N, Mashiba S, Ueda N. J. Org. Chem. 1998; 63: 7931
    • 17a Chan A, Scheidt KA. Org. Lett. 2005; 7: 905
    • 17b Sohn SS, Bode JW. Org. Lett. 2005; 7: 3873
    • 17c Wang MH, Barsoum D, Schwamb CB, Cohen DT, Goess BC, Riedrich M, Chan A, Maki BE, Mishra RK, Scheidt KA. J. Org. Chem. 2017; 82: 4689
    • 18a Reynolds NT, Read de Alaniz J, Rovis T. J. Am. Chem. Soc. 2004; 126: 9518
    • 18b Reynolds NT, Rovis T. J. Am. Chem. Soc. 2005; 127: 16406
  • 19 Clough S, Gupton J, Ligali A, Roberts M, Driscoll D, Annett S, Hewitt A, Hudson M, Jackson E, Miller R, Norwood B, Kanters R, Wyre H, Petruzzi H. Tetrahedron 2005; 61: 7554
  • 20 Tschaen BA, Schmink JR, Molander GA. Org. Lett. 2013; 15: 500
  • 21 Lerebours R, Wolf C. J. Am. Chem. Soc. 2006; 128: 13052
  • 22 Yasukawa T, Yang X, Kobayashi S. Org. Lett. 2018; 20: 5172
  • 23 Gowrisankar S, Seayad J. Asian J. Org. Chem. 2015; 4: 521
  • 24 Gruber AS, Zim D, Ebeling G, Monteiro AL, Dupont J. Org. Lett. 2000; 2: 1287
  • 25 Mantecon S, Vaquero JJ, Alvarez-Builla J, de la Puente ML, Espinosa JF, Ezquerra J. Org. Lett. 2003; 5: 3791
  • 26 Littke AF, Fu GC. J. Org. Chem. 1999; 64: 10
  • 27 Pastre JC, Correia CR. D. Adv. Synth. Catal. 2009; 351: 1217
  • 28 Oi S, Honma Y, Inoue Y. Org. Lett. 2002; 4: 667
    • 29a O’Brien CJ, Lavigne F, Coyle EE, Holohan AJ, Doonan BJ. Chem. Eur. J. 2013; 19: 5854
    • 29b Li J, Qian W, Zhang Y. Tetrahedron 2004; 60: 5793
  • 30 Seifert F, Drikermann D, Steinmetzer J, Zi Y, Kupfer S, Vilotijevic I. Org. Biomol. Chem. 2021; 19: 6092