Sigmatropic reaction

A sigmatropic reaction in organic chemistry is a pericyclic reaction wherein the net result is one σ-bond is changed to another σ-bond in an uncatalyzed intramolecular reaction.[1] The name sigmatropic is the result of a compounding of the long-established sigma designation from single carbon–carbon bonds and the Greek word tropos, meaning turn. In this type of rearrangement reaction, a substituent moves from one part of a π-bonded system to another part in an intramolecular reaction with simultaneous rearrangement of the π system.[2] True sigmatropic reactions are usually uncatalyzed, although Lewis acid catalysis is possible. Sigmatropic reactions often have transition-metal catalysts that form intermediates in analogous reactions. The most well-known of the sigmatropic rearrangements are the [3,3] Cope rearrangement, Claisen rearrangement, Carroll rearrangement, and the Fischer indole synthesis.

Overview of sigmatropic shifts

Woodward–Hoffman sigmatropic shift nomenclature

Sigmatropic rearrangements are concisely described by an order term [i,j], which is defined as the migration of a σ-bond adjacent to one or more π systems to a new position (i−1) and (j−1) atoms removed from the original location of the σ-bond.[3] When the sum of i and j is an even number, this is an indication of the involvement of a neutral, all C atom chain. An odd number is an indication of the involvement of a charged C atom or of a heteroatom lone pair replacing a CC double bond. Thus, [1,5] and [3,3] shifts become [1,4] and [2,3] shifts with heteroatoms, while preserving symmetry considerations. Hydrogens are omitted in the third example for clarity.

A convenient means of determining the order of a given sigmatropic rearrangement is to number the atoms of the bond being broken as atom 1, and then count the atoms in each direction from the broken bond to the atoms that form the new σ-bond in the product, numbering consecutively. The numbers that correspond to the atoms forming the new bond are then separated by a comma and placed within brackets to create the sigmatropic reaction order descriptor.[4]

In the case of hydrogen atom migrations, a similar technique may be applied. When determining the order of a sigmatropic shift involving a hydrogen atom migration it is critical to count across all atoms involved in the reaction rather than only across the closest atoms. For example, the following hydrogen atom migration is of order [1,5], attained by counting counterclockwise through the π system, rather than the [1,3] order designation through the ring CH2 group that would mistakenly result if counted clockwise.

As a general approach, one can simply draw the transition state of the reaction. For a sigmatropic reaction, the transition state will consist of two fragments, joined together by the forming and breaking σ-bonds. The sigmatropic reaction is named as a [i,j]-sigmatropic rearrangement (i ≤ j) if these two fragments consist of i and j atoms. This is illustrated below, with the relevant fragments shown in color.

Suprafacial and antarafacial shifts

In principle, all sigmatropic shifts can occur with either a retention or inversion of the geometry of the migrating group, depending upon whether the original bonding lobe of the migrating atom or its other lobe is used to form the new bond.[4]

In cases of stereochemical retention, the migrating group translates without rotation into the bonding position, while in the case of stereochemical inversion the migrating group both rotates and translates to reach its bonded conformation.

However, another stereochemical transition effect equally capable of producing inversion or retention products is whether the migrating group remains on the original face of the π system after rebonding or instead transfers to the opposite face of the π system. If the migrating group remains on the same face of the π system, the shift is known as suprafacial, while if the migrating group transfers to the opposite face is called an antarafacial shift,[3] which are impossible for transformations that occur within small- or medium-sized rings.

Classes of sigmatropic rearrangements

Thermal hydride shifts

In a thermal [1,3] hydride shift, a hydride moves three atoms. The Woodward–Hoffmann rules dictate that it would proceed in an antarafacial shift. Although such a shift is symmetry allowed, the Mobius topology required in the transition state prohibits such a shift because it is geometrically impossible, which accounts for the fact that enols do not isomerize without an acid or base catalyst.[4]

Impossible shift

Thermal alkyl shifts

Thermal alkyl [1,3] shifts, similar to [1,3] hydride shifts, must proceed antarafacially. Here the geometry of the transition state is prohibitive, but an alkyl group, due to the nature of its orbitals, can invert its geometry, form a new bond with the back lobe of its sp3 orbital, and therefore proceed via a suprafacial shift. These reactions are still not common in open-chain compounds because of the highly ordered nature of the transition state, which is more readily achieved in cyclic molecules.[4]

[1,3] Alkyl shifts

Photochemical [1,3] shifts

Photochemical [1,3] shifts should proceed through suprafacial shifts; however, most are non-concerted because they proceed through a triplet state (i.e., have a diradical mechanism, to which the Woodward-Hoffmann rules do not apply).[4]

[1,5] shifts

A [1,5] shift involves the shift of 1 substituent (hydride, alkyl, or aryl) down 5 atoms of a π system. Hydrogen has been shown to shift in both cyclic and open-chain compounds at temperatures at or above 200 ˚C.[4] These reactions are predicted to proceed suprafacially, via a Hückel-topology transition state.

[1,5] hydride shift in a cyclic system

Photoirradiation would require an antarafacial shift of hydrogen. Although rare, there are examples where antarafacial shifts are favored:[5]

Antarafacial [1,5] hydride shift

In contrast to hydrogen [1,5] shifts, there have never been any observed [1,5] alkyl shifts in an open-chain compound.[4] Several studies have, however, been done to determine rate preferences for [1,5] alkyl shifts in cyclic systems: carbonyl and carboxyl> hydride> phenyl and vinyl>> alkyl.[6][7]

Alkyl groups undergo [1,5] shifts very poorly, usually requiring high temperatures, however, for cyclohexadiene, the temperature for alkyl shifts isn't much higher than that for carbonyls, the best migratory group. A study showed that this is because alkyl shifts on cyclohexadienes proceed through a different mechanism. First the ring opens, followed by a [1,7] shift, and then the ring reforms electrocyclically:[8]

alkyl shift on cyclohexadiene

This same mechanistic process is seen below, without the final electrocyclic ring-closing reaction, in the interconversion of lumisterol to vitamin D2.

[1,7] shifts

[1,7] sigmatropic shifts are predicted by the Woodward–Hoffmann rules to proceed in an antarafacial fashion, via a Mobius topology transition state. An antarafacial [1,7] shift is observed in the conversion of lumisterol to vitamin D2, where following an electrocyclic ring opening to previtamin D2, a methyl hydrogen shifts.[9]

conversion of Lumisterol to Vitamin D2

Bicyclic nonatrienes also undergo [1,7] shifts in a so-called walk rearrangement,[10] which is the shift of divalent group, as part of a three-membered ring, in a bicyclic molecule.

walk rearrangement of bicycle nonatriene

[3,3] shifts

[3,3] sigmatropic shifts are well studied sigmatropic rearrangements. The Woodward–Hoffman rules predict that these six-electron reactions would proceed suprafacially, via a Hückel topology transition state.

Claisen rearrangement

Discovered in 1912 by Rainer Ludwig Claisen, the Claisen rearrangement is the first recorded example of a [3,3]-sigmatropic rearrangement.[11][12][13] This rearrangement is a useful carbon-carbon bond-forming reaction. An example of Claisen rearrangement is the [3,3] rearrangement of an allyl vinyl ether, which upon heating yields a γ,δ-unsaturated carbonyl. The formation of a carbonyl group makes this reaction, unlike other sigmatropic rearrangements, inherently irreversible.

The Claisen rearrangement
Aromatic Claisen rearrangement

The ortho-Claisen rearrangement involves the [3,3] shift of an allyl phenyl ether to an intermediate which quickly tautomerizes to an ortho-substituted phenol.

Aromatic Claisen rearrangement

When both the ortho positions on the benzene ring are blocked, a second [3,3] rearrangement will occur. This para-Claisen rearrangement ends with the tautomerization to a tri-substituted phenol.

Para-Claisen rearrangement

Cope rearrangement

The Cope rearrangement is an extensively studied organic reaction involving the [3,3] sigmatropic rearrangement of 1,5-dienes.[14][15][16] It was developed by Arthur C. Cope. For example, 3,4-dimethyl-1,5-hexadiene heated to 300 °C yields 2,6-octadiene.

The Cope rearrangement of 3,4-dimethyl-1,5-hexadiene
Oxy-Cope rearrangement

In the oxy-Cope rearrangement, a hydroxyl group is added at C3 forming an enal or enone after keto-enol tautomerism of the intermediate enol:[17]

Oxy-Cope rearrangement

Carroll rearrangement

The Carroll rearrangement is a rearrangement reaction in organic chemistry and involves the transformation of a β-keto allyl ester into a α-allyl-β-ketocarboxylic acid.[18] This organic reaction is accompanied by decarboxylation and the final product is a γ,δ-allylketone. The Carroll rearrangement is an adaptation of the Claisen rearrangement and effectively a decarboxylative allylation.

Carroll Rearrangement

Fischer indole synthesis

The Fischer indole synthesis is a chemical reaction that produces the aromatic heterocycle indole from a (substituted) phenylhydrazine and an aldehyde or ketone under acidic conditions.[19][20] The reaction was discovered in 1883 by Hermann Emil Fischer.

The Fischer indole synthesis

The choice of acid catalyst is very important. Brønsted acids such as HCl, H2SO4, polyphosphoric acid and p-toluenesulfonic acid have been used successfully. Lewis acids such as boron trifluoride, zinc chloride, iron(III) chloride, and aluminium chloride are also useful catalysts.

Several reviews have been published.[21][22][23]

[5,5] Shifts

Similar to [3,3] shifts, the Woodward-Hoffman rules predict that [5,5] sigmatropic shifts would proceed suprafacially, Hückel topology transition state. These reactions are rarer than [3,3] sigmatropic shifts, but this is mainly a function of the fact that molecules that can undergo [5,5] shifts are rarer than molecules that can undergo [3,3] shifts.[4]

[5,5] shift of phenyl pentadienyl ether

[2,3] shifts

An example of a 2,3-sigmatropic rearrangement is the 2,3-Wittig rearrangement:

Walk rearrangements

The migration of a divalent group, such as O, S, N–R, or C–R2, which is part of a three-membered ring in a bicyclic molecule, is commonly referred to as a walk rearrangement. This can be formally characterized according to the Woodward-Hofmann rules as being a (1, n) sigmatropic shift.[24] An example of such a rearrangement is the shift of substituents on tropilidenes (1,3,5-cycloheptatrienes). When heated, the pi-system goes through an electrocyclic ring closing to form bicycle[4,1,0]heptadiene (norcaradiene). Thereafter follows a [1,5] alkyl shift and an electrocyclic ring opening.

norcaradiene rearrangement

Proceeding through a [1,5] shift, the walk rearrangement of norcaradienes is expected to proceed suprafacially with a retention of stereochemistry. Experimental observations, however, show that the 1,5-shifts of norcaradienes proceed antarafacially.[25] Theoretical calculations found the [1,5] shift to be a diradical process, but without involving any diradical minima on the potential energy surface.[26]

See also
  • 2,3-sigmatropic rearrangement
  • NIH shift
  • Frontier molecular orbital theory

References
  1. Carey, F.A. and R.J. Sundberg. Advanced Organic Chemistry Part A ISBN 0-306-41198-9
  2. "Sigmatropic Rearrangements". Chemistry LibreTexts.
  3. Woodward, R.B.; Hoffmann, R. The Conservation of Orbital Symmetry. Verlag Chemie Academic Press. 2004. ISBN 0-89573-109-6.
  4. Miller, Bernard. Advanced Organic Chemistry. 2nd Ed. Upper Saddle River: Pearson Prentice Hall. 2004. ISBN 0-13-065588-0
  5. Kiefer, E.F.; Tana, C.H. J. Am. Chem. Soc., 1969, 91, 4478. doi:10.1021/ja01044a027
  6. Fields, D.J.; Jones, D.W.; Kneen, G. Chemical Communications 1976. 873 – 874. doi:10.1039/C39760000873
  7. Miller, L.L.; Greisinger, R.; Boyer, R.F. J. Am. Chem. Soc. 1969. 91. 1578. doi:10.1021/ja01034a076
  8. Schiess, P.; Dinkel, R. Tetrahedron Letters, 1975, 16, 29, 2503. doi:10.1016/0040-4039(75)80050-5
  9. Carey, Francis A; Sundberg, Richard J (2000). Advanced Organic Chemistry. Part A: Structure and Mechanisms (4th ed.). New York: Kluwer Academic/Plenum. p. 625. ISBN 0-306-46242-7.
  10. Klaerner, F.G. Agnew. Chem. Intl. Ed. Eng., 1972, 11, 832.doi:10.1002/anie.197208321
  11. Claisen, L.; Ber. 1912, 45, 3157. doi:10.1002/cber.19120450348
  12. Claisen, L.; Tietze, E.; Chemische Berichte 1925, 58, 275. doi:10.1002/cber.19250580207
  13. Claisen, L.; Tietze, E.; Chemische Berichte 1926, 59, 2344. doi:10.1002/cber.19260590927
  14. Cope, A. C.; et al. J. Am. Chem. Soc. 1940, 62, 441. doi:10.1021/ja01859a055
  15. Hoffmann, R.; Stohrer, W. D. J. Am. Chem. Soc. 1971, 93, 25, 6941–6948. doi:10.1021/ja00754a042
  16. Dupuis, M.; Murray, C.; Davidson, E. R. J. Am. Chem. Soc. 1991, 113, 26, 9756–9759. doi:10.1021/ja00026a007
  17. Berson, Jerome A.; Jones, Maitland. J. Am. Chem. Soc. 1964, 86, 22, 5019–5020. doi:10.1021/ja01076a067
  18. Carrol, M. F. Journal of the Chemical Society 1940, 704–706. doi:10.1039/JR9400000704.
  19. Fischer, E.; Jourdan, F. Chemische Berichte 1883, 16, 2241.doi:10.1002/cber.188301602141
  20. Fischer, E.; Hess, O. Chemische Berichte 1884, 17, 559. doi:10.1002/cber.188401701155
  21. van Orden, R. B.; Lindwell, H. G. Chem. Rev. 1942, 30, 69–96. doi:10.1021/cr60095a004
  22. Robinson, B. Chem. Rev. 1963, 63, 373–401. doi:10.1021/cr60224a003
  23. Robinson, B. Chem. Rev. 1969, 69, 227–250. doi:10.1021/cr60262a003
  24. Jensen, F. J. Am. Chem. Soc., 1989, 111, 13, 4643 – 4647. doi:10.1021/ja00195a018
  25. Klarner, F.G. Topics in Stereochemistry, 1984, 15, 1–42. ISSN 0082-500X
  26. Kless, A.; Nendel, M.; Wilsey, S.; Houk, K. N. J. Am. Chem. Soc., 1999, 121, 4524. doi:10.1021/ja9840192
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.