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Pictet-Spengler route to Praziquantel
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3rd August 2010 @ 09:28
2. step for the preparation of 1,1-Binaphthyl-2,2-disulfonate – a strong achiral Brønstedt-acid, intended for determination and optimization of the reaction conditions for the acid-catalyzed Pictet-Spengler reaction [1,2] 1. step: preparation of the starting material -> [url=http://www.ourexperiment.org/racemic_pzq/567]see [b]MW45-1[/b][/url] [data=size:500x180]395[/data] [b]Hazard and Risk Assessment:[/b] Reaction Class: 2 Hazards: T toxic Risk rating: U = Unlikely Start time: 1:00 PM 03/08/2010 End time: 2:20 PM 03/08/2010 [b]Procedure:[/b] [2] [url=http://www.ourexperiment.org/racemic_pzq/567][b]MW45-1[/b][/url] (500 mg, 1.09 mmol) was placed in a roundbottom flask and heated in a heating mantle to 250°C for 80 min. The dark brown solid was dissolved in chloroform and purified by column chromatography (silica gel, CHCl3; 100%). [b]References:[/b] [url=http://dx.doi.org/10.1021/ja806875c][1] “Pyridinium 1,1′-Binaphthyl-2,2′-disulfonates as Highly Effective Chiral Brønsted Acid−Base Combined Salt Catalysts for Enantioselective Mannich-Type Reaction”, M. Hatano, T. Maki, K. Moriyama, M. Arinobe and K. Ishihara, J. Am. Chem. Soc. 2008, 130, 16858–16860; DOI: 10.1021/ja806875c. [/url] [url=http://www3.interscience.wiley.com/journal/122382952/abstract][2] “A Powerful Chiral Counteranion Motif for Asymmetric Catalysis”, P. García-García, F. Lay, P. García-García, C. Rabalakos, B. List, Angew. Chem. Int. Ed. 2009, 48, 4363 –4366; DOI: 10.1002/anie.200901768.[/url] See following experiment: [*] [url=http://www.ourexperiment.org/racemic_pzq/587]Preparation of 1,1’-Binaphthalene-2,2’-disulfonic acid (MW45-3)[/url] [b]Procedure from the reference:[/b] [2] [i](R)-3,3'-Bis[3,5-bis(trifluoromethyl)phenyl]-1,1'-binaphthyl-2,2'-diyl-S,S'-bis(N,N-dimethylthiocarbamate) (13):[/i] O-Thiocarbamate 12 (2.31 g, 2.61 mmol) was placed into a dram glass vial under argon and heated in a metal block to 250 °C for 80 min. The resulting crude product was purified by column chromatography using hexanes/ethyl acetate (95/5) as eluent to afford 13 (2.19 g, 95% yield).
Attached Files
Reaction Scheme
1H NMR MW45-2
1H NMR MW45-2 JCAMP-DX.dx
IR MW42-2
IR MW45-2