|   Catalyzed Organic Reactions in Ionic Liquids |
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| Speaker: |
William M. Nelson
| Illinois Department of Natural Resources | Waste Management & Research Center |
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| Date: | Friday, March 22, 2002 |
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| Location:   |
Chicago Marriott O'Hare
(Same as main meeting) |
Topical Group: 5:30-6:30 P.M.
Social Hour: 6:00- 7:00 P.M.
Dinner: 7:00 P.M.
Meeting: 8:00 P.M.
The chemical industry is under considerable pressure to replace many of the volatile organic compounds (VOCs) that are currently used as solvents in organic synthesis. This is an important driving force in the quest for novel reaction media. Green chemistry principles provide the guidelines (in broad terms) for chemists engaged in organic synthesis. The key to waste minimization in chemistry is the widespread substitution of classical 'stoichiometric' syntheses by atom efficient, catalytic alternatives. Examples will illustrate two ways in which catalyzed organic reactions in ionic liquids exemplify green chemistry. Firstly, they yield significant rate enhancement and high yield/selectivity. This can be demonstrated across a broad range of reactions. Secondly, they can improve the “greenness” of the syntheses: less energy expenditure, improved atom-economy, reduced solvent distribution into environment, and reduced environmental absorption. The range of reaction types run in ionic liquids will include name organic reactions (e.g., Diels-Alder and Friedel-Crafts) and general organic transformations e.g., (benzoylation, epoxide opening, arylations, and coupling).