Syntheses of Isoquinoline and Substituted Quinolines in Charged Microdroplets.

A Pomeranz-Fritsch synthesis of isoquinoline and Friedländer and Combes syntheses of substituted quinolines were conducted in charged microdroplets produced by an electrospray process at ambient temperature and atmospheric pressure. In the bulk phase, all of these reactions are known to take a long time ranging from several minutes to a few days and to require very high acid concentrations. In sharp contrast, the present report provides clear evidence that all of these reactions occur on the millisecond timescale in the charged microdroplets without the addition of any external acid. Decreasing the droplet size and increasing the charge of the droplet both strongly contribute to reaction rate acceleration, suggesting that the reaction occurs in a confined environment on the charged surface of the droplet.

[1]  J. Born Mechanism of formation of benzo[g]quinolones via the Combes reaction , 1972 .

[2]  Shibdas Banerjee Induction of protein conformational change inside the charged electrospray droplet. , 2013, Journal of mass spectrometry : JMS.

[3]  G. Guillena,et al.  Solvent-free enantioselective Friedländer condensation with wet 1,1'-binaphthalene-2,2'-diamine-derived prolinamides as organocatalysts. , 2013, The Journal of organic chemistry.

[4]  E. Fattorusso,et al.  Modern Alkaloids : Structure, Isolation, Synthesis and Biology , 2008 .

[5]  Joh. Müller,et al.  Eine neue Modifikation der Isochinolinsynthese nach Pomeraz-Fritsch , 1948 .

[6]  I. Leito,et al.  Towards the electrospray ionization mass spectrometry ionization efficiency scale of organic compounds. , 2008, Rapid communications in mass spectrometry : RCM.

[7]  A. Gomez,et al.  Generation by electrospray of monodisperse water droplets for targeted drug delivery by inhalation , 1994 .

[8]  Shibdas Banerjee,et al.  Selective Deletion of the Internal Lysine Residue from the Peptide Sequence by Collisional Activation , 2012, Journal of The American Society for Mass Spectrometry.

[9]  M. Mann,et al.  Electrospray ionization for mass spectrometry of large biomolecules. , 1989, Science.

[10]  Allis S. Chien,et al.  Detecting reaction intermediates in liquids on the millisecond time scale using desorption electrospray ionization. , 2011, Angewandte Chemie.

[11]  M. Oss,et al.  Electrospray ionization efficiency scale of organic compounds. , 2010, Analytical chemistry.

[12]  J. Smid Die Struktur solvatisierter Ionenpaare , 1972 .

[13]  R. Cooks,et al.  Accelerated C–N Bond Formation in Dropcast Thin Films on Ambient Surfaces , 2012, Journal of The American Society for Mass Spectrometry.

[14]  C. Pomeranz Über eine neue Isochinolinsynthese , 1893 .

[15]  R. Cooks,et al.  Accelerated carbon-carbon bond-forming reactions in preparative electrospray. , 2012, Angewandte Chemie.

[16]  Andrew D Griffiths,et al.  Enhanced chemical synthesis at soft interfaces: a universal reaction-adsorption mechanism in microcompartments. , 2014, Physical review letters.

[17]  G. Siuzdak,et al.  Electrospray and MALDI mass spectrometry in the identification of spermicides in criminal investigations. , 1999, Journal of forensic sciences.

[18]  R. Grigg,et al.  8-Methylquinoline palladacycles: stable and efficient catalysts for carbon–carbon bond formation , 2005 .

[19]  K. C. Majumdar,et al.  Heterocycles in Natural Product Synthesis: MAJUMDAR:HETEROCYCLES O-BK , 2011 .

[20]  S. Tu,et al.  Rapid and efficient synthesis of poly-substituted quinolines assisted by p-toluene sulphonic acid under solvent-free conditions: comparative study of microwave irradiation versus conventional heating. , 2006, Organic & biomolecular chemistry.

[21]  P. Friedlaender Ueber o‐Amidobenzaldehyd , 1882 .

[22]  A. Shaabani,et al.  Triflouroacetic Acid as an Efficient Catalyst for the Synthesis of Quinoline , 2007 .

[23]  Abdelouahid Samadi,et al.  Recent advances in the Friedländer reaction. , 2009, Chemical reviews.

[24]  J. Smid Structure of Ion Pair Solvation Complexes , 1972 .

[25]  J. Bobbitt,et al.  Synthesis of Heterocycles Using Aminoacetals , 1987 .

[26]  A. Kost,et al.  Closure of the pyridine ring in the combes quinoline synthesis (Review) , 1992 .

[27]  Joseph Sloop Quinoline formation via a modified Combes reaction: examination of kinetics, substituent effects, and mechanistic pathways , 2009 .

[28]  Shibdas Banerjee,et al.  Evidence of Molecular Fragmentation inside the Charged Droplets Produced by Electrospray Process , 2011, Journal of the American Society for Mass Spectrometry.

[29]  R. Cooks,et al.  Accelerated bimolecular reactions in microdroplets studied by desorption electrospray ionization mass spectrometry , 2011 .

[30]  F. Tureček,et al.  Acidity Determination in Droplets Formed by Electrospraying Methanol-Water Solutions , 1994 .

[31]  J. Smid The discovery of two kinds of ion pairs , 2004 .

[32]  Shibdas Banerjee,et al.  Non-covalent dimers of the lysine containing protonated peptide ions in gaseous state: electrospray ionization mass spectrometric study. , 2010, Journal of mass spectrometry : JMS.

[33]  J. Fenn,et al.  Ion formation from charged droplets: Roles of geometry, energy, and time , 1993, Journal of the American Society for Mass Spectrometry.

[34]  D. Werner,et al.  One-Pot FriedländerQuinoline Synthesis: Scope and Limitations , 2010 .

[35]  Hong Gil Nam,et al.  Microdroplet fusion mass spectrometry for fast reaction kinetics , 2015, Proceedings of the National Academy of Sciences.

[36]  K. Nagaiah,et al.  Silver Phosphotungstate: A Novel and Recyclable Heteropoly Acid for Friedländer Quinoline Synthesis , 2004 .