Chemistry 251 Laboratory -- Spring 2001
Enantioselective Ibuprofen Project Home Page

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Last updated on 2/13/01

Index

Racemic Synthesis of Ibuprofen

Faculty Mentor: John Hanson

Reference: Cleij, M.; Archelas, A.; Furstoss, R. J. Org. Chem. 1999, 64, 5029-5035.

Ibuprofen is the active ingredient in a number of over the counter pain relievers, e.g. Advil, Motrin, and Nuprin. It is one of the top-ten drugs sold worldwide, and, although it has been shown that only the S enantiomer has the desired biological activity, it is currently sold as the racemate. There are actually two syntheses worth exploring here. The first, a synthesis of the racemate, begins with reaction of 4-isobutylacetophenone with the sulfur ylide produced by deprotonation of trimethylsulfonium iodide to yield an epoxide. (You should look this reaction up in an advanced organic text, e.g. the one by Jerry March.) Last year we found that BF3Et2O catalyzed rearrangement of the epoxide to give the aldehyde worked well. What remains to be explored is the oxidation of this aldehyde to give the racemic Ibuprofen. An enantioselective synthesis of Ibuprofen could be accomplished by first performing a Wittig reaction to give the alkene and then performing an enantioselective epoxidation. The epoxide is then opened reductively by treatment with H2 and Pd catalyst to give an alcohol that is then oxidized to the acid, Ibuprofen, using KMnO4.




Students Working on This Project

Lab Day Name E-mail
Monday Jocelyn Takayesu jtakayesu@ups.edu
Monday Jen Itano jitano@ups.edu
Tuesday
Tuesday
Wednesday
Wednesday
Thursday Aft.
Thursday Aft.
Thursday Eve. Andy Anson aanson@ups.edu
Thursday Eve. Eric Johnson eajohnson@ups.edu



Table of Reagents and Amounts Available for this Project

The table below lists the chemicals that we will have available for this project. If you need something that is not on this list, consult with the mentor for your project. Also note the "Amount/group" column. This is the total amount of material available for each group to use on the project.
Reagent Source Amount/group Location Comments
4-isobutylacetophenone Lancaster
Cat. # 6284
5 g TA room
Methyltriphenylphosphonium bromide Aldrich
Cat. #13,007-9
10 g TA room Irritant, Hygroscopic
Butyllithium (1.6 M in Hexanes) Aldrich
Cat. #18,617-1
20 mL TA room Flammable Liquid, Moisture Sensitive
DMSO (Dimethyl sulfoxide) TA room Wear gloves when handling DMSO. It is readily absorbed through the skin!