Química Nova (Jan 2012)

Resolução do ibuprofeno: um projeto para disciplina de química orgânica experimental

  • Adriano L. Romero,
  • Lúcia H. B. Baptistella,
  • Fernando Coelho,
  • Paulo M. Imamura

DOI
https://doi.org/10.1590/S0100-40422012000800031
Journal volume & issue
Vol. 35, no. 8
pp. 1680 – 1685

Abstract

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A practical and didactic sequence of experiments was proposed to illustrate the stereochemistry concept, optically active compounds, resolution of racemates, and use of the NMR technique, including 2D-COSY for identification of organic compounds, on a laboratory course for undergraduate students. The sequence was: extractions of racemic ibuprofen and chiral naproxen from commercial tablets; syntheses of diastereoisomeric amides reacting chiral (S)-(-)-α-methylbenzylamine with (±)-ibuprofen; separation and determination of absolute configuration of amides by ¹H NMR spectroscopy and GC analysis, and hydrolysis of amides to obtain (+)- and (-)-ibuprofen.

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