Diels–Alder reaction

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Diels–Alder reaction
Named after Otto Diels
Kurt Alder
Reaction type Cycloaddition
Diels-alder (1,3-butadiene - Ethylene).png
conjugated (substituted) Diene
(substituted) Olefin
(substituted) Cyclohexene
RSC ontology ID RXNO:0000006 YesY

The Diels–Alder reaction (DA) is a chemical reaction between organic compounds. The reaction causes the compounds to form a new six-sided compound. This is called a cyclohexene. A conjugated diene joins with an alkene to make the cyclohexene. This compound looks like a ring.[1][2]

This reaction was discovered by Otto Diels and Kurt Alder in 1928. In 1950, they were given the Nobel Prize in Chemistry for their work on this reaction. The DA reaction is very useful as it means cyclohexenes can be made with very little energy. Cyclohexenes are used to make complex organic molecules.[3][4][5][6] One of the first uses of the DA reaction was to make insecticides.[7]

The DA reaction makes a new hexagonal ring-shaped compound. A compound with two double bonds which are one carbon atom apart from each other is joined to another compound with at least one double bond. A DA reaction can also happen if some of the atoms in the newly formed ring are not carbon. Some of the DA reactions are reversible. The reaction caused during this breaking up of the cyclic system is called the retro-Diels–Alder. These retro-Diels–Alder compounds are often seen when they are analyzed by mass spectrometry.

Some chemists call the Diels–Alder reaction the 'Mona Lisa' of organic reactions. Like the simple smile on the painting, the reaction may be far more complex than chemists have so far discovered.[8]

Lewis acids (AlCl3, ZnCl2, and others) act as catalysts to the reaction.

References[change | change source]

  1. Diels O. & Alder K. 1928. Synthesen in der hydroaromatischen Reihe. Justus Liebig's Annalen der Chemie 460: 98–122. doi:10.1002/jlac.19284600106.
  2. Diels O. & Alder K. 1929. Synthesis in the hydroaromatic series, IV. Announcement: the rearrangement of malein acid anhydride on arylated diene, triene and fulvene. Chemische Berichte, 62, 2081 & 2087.
  3. Kloetzel M.C. 1948. Org. React. 4, 1–59
  4. Holmes H.L. 1948. Org. React. 4, 60–173.
  5. Kagan H.B. & Riant O. 1992. Catalytic asymmetric Diels Alder reactions. Chemical Reviews 92 (5): 1007. doi:10.1021/cr00013a013
  6. Nicolaou K.C. etal 2002. The Diels–Alder Reaction in total synthesis. Angew. Chem. Int. Ed. 41, 1668–1698. doi:10.1002/1521-3773(20020517)41:10<1668::AID-ANIE1668>3.0.CO;2-Z
  7. "Diels-Alder reaction". McGraw-Hill Concise Encyclopedia of Science and Technology. 2006. http://www.credoreference.com/entry/conscitech/diels_alder_reaction. Retrieved 30 July 2011.
  8. Nye, Mary Jo (December 2006). "Working tools for theoretical chemistry: Polanyi, eyring, and debates over the “semiempirical method”". Journal of Computational Chemistry 28 (1): 3. http://onlinelibrary.wiley.com/doi/10.1002/jcc.20527/pdf. Retrieved 30 July 2011.

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