Reference : The step-by-step Robinson annulation of chalcone and ethyl acetoacetate - An advanced...
Scientific journals : Article
Social & behavioral sciences, psychology : Education & instruction
Physical, chemical, mathematical & earth Sciences : Chemistry
http://hdl.handle.net/2268/15417
The step-by-step Robinson annulation of chalcone and ethyl acetoacetate - An advanced undergraduate project in organic synthesis and structural analysis
English
Delaude, Lionel mailto [Université de Liège - ULg > > Chimie macromoléculaire et catalyse organique >]
Grandjean, Jean mailto [Université de Liège - ULg > > Chimie organique et spectroscopie multinucléaire (COSM) >]
Noels, Alfred mailto [Université de Liège - ULg > Services généraux (Faculté des sciences) > Relations académiques et scientifiques (Sciences) >]
2006
Journal of Chemical Education
Amer Chemical Soc
83
8
1225-1228
Yes (verified by ORBi)
International
0021-9584
Washington
DC
[en] Catalysis ; Chirality / Optical Activity ; Conformational Analysis ; Diastereomers ; Hands-On Learning ; Manipulatives ; IR Spectroscopy ; Laboratory Instruction ; NMR Spectroscopy ; Second-Year Undergraduate ; Stereochemistry ; Upper-Division Undergraduate
[en] The Robinson annulation is a three-step process involving a Michael addition followed by an internal aldol condensation and a dehydration. Under appropriate experimental conditions, it is possible to stop the reaction after every step and to isolate the three products separately. This feature is particularly attractive in the frame of an organic chemistry course. It allows students to confirm experimentally the validity of the stepwise mechanism and to get a more thorough understanding of the whole process. It also permits them to synthesize a rich set of related molecules that can be compared and characterized through various analytical techniques. Thus, a stoichiometric mixture of chalcone and ethyl acetoacetate was reacted in ethanol. Depending on the quantity of barium hydroxide monohydrate used as catalyst, the reaction time, and the temperature, three different products were obtained. Their full IR, 1H, 13C, COSY, NOESY, and HETCOR NMR spectra are supplied. Examination of the spectroscopic data helps uncover many challenging structural analysis problems. Among them, the diastereoselective formation of chiral centers during the annulation process, the distinction between axial and equatorial substituents on a cyclohexane ring, and the possibility of a keto-enol tautomerism are extensively discussed.
http://hdl.handle.net/2268/15417

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