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

Cope rearrangement
Named after Arthur C. Cope
Reaction type Rearrangement reaction
Organic Chemistry Portal cope-rearrangement
RSC ontology ID RXNO:0000028
The Cope rearrangement of 3-methyl-1,5-hexadiene

The Cope rearrangement causes the fluxional states of the molecules in the bullvalene family.



The Cope rearrangement is the prototypical example of a concerted sigmatropic rearrangement. It is classified as a [3,3]-sigmatropic rearrangement with the Woodward-Hoffmann symbol [π2s+σ2s+π2s] and is therefore thermally allowed. It is sometimes useful to think of it as going through a transition state energetically and structurally equivalent to a diradical, although it should be emphasized that the diradical is not usually a true intermediate (potential energy minimum).[5] The chair transition state illustrated here is preferred in open-chain systems (as shown by the Doering-Roth experiments). However, conformationally constrained systems like cis-1,2-divinylcyclopropanes can undergo the rearrangement in the boat conformation.


It is currently generally accepted that most Cope rearrangements follows an allowed concerted route through a Hückel aromatic transition state and a diradical intermediate is not formed. However, the concerted reaction can often be asynchronous and electronically perturbed systems may have considerable diradical character at the transition state.[6] A representative illustration of the transition state of the Cope rearrangement of the electronically neutral 1,5-hexadiene is presented below. Here one can see that the two π-bonds are breaking while two new π-bonds are forming, and simultaneously the σ-bond is breaking while a new σ-bond is forming. In contrast to the Claisen rearrangement, Cope rearrangements without strain release or electronic perturbation are often close to thermally neutral, and may therefore reach only partial conversion due to an insufficiently favorable equilibrium constant. In the case of hexa-1,5-diene, the rearrangement is degenerate (the product is identical to the starting material), so K = 1 by necessity.


In asymmetric dienes one often needs to consider the stereochemistry, which in the case of pericyclic reactions, such as the Cope rearrangement, can be predicted with the Woodward-Hoffmann rules and consideration of the preference for the chair transition state geometry.


The rearrangement is widely used in organic synthesis. It is symmetry-allowed when it is suprafacial on all components. The transition state of the molecule passes through a boat or chair like transition state. An example of the Cope rearrangement is the expansion of a cyclobutane ring to a 1,5-cyclooctadiene ring:


In this case, the reaction must pass through the boat transition state to produce the two cis double bonds. A trans double bond in the ring would be too strained. The reaction occurs under thermal conditions. The driving force of the reaction is the loss of strain from the cyclobutane ring.

Oxy-Cope rearrangement and its anionic variantEdit

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:[7][8]


In its originally form, the reaction needs very high temperatures to proceed at a reasonable rate. However, in 1975, Evans and Golob showed that deprotonation of oxy-Cope substrates with strong base to form the corresponding potassium alkoxide resulted in rate accelerations of 1010 to 1017 relative to the reaction conducted under neutral conditions. This allows the reaction to be conducted at room temperature or even 0 °C. Typically potassium hydride and 18-crown-6 are employed in order to generate a fully dissociated potassium alkoxide:[9]


The diastereomer of the starting material shown above with an equatorial vinyl group does not react, providing evidence of the concerted nature of this reaction. Nevertheless, the transition state of the reaction is believed to have a high degree of diradical character. Consequently, the anion-accelerated oxy-Cope reaction can proceed with high efficiency even in systems that do not permit efficient orbital overlap, as seen in this example from the synthesis periplanone B by Schreiber and Santini:[10]


The authors remark that the corresponding neutral oxy-Cope and siloxy-Cope rearrangements failed, giving only elimination products at 200 °C.


Another variation of the Cope rearrangement is the heteroatom Cope reactions such as the aza-Cope rearrangements. Another widely studied [3, 3] sigmatropic rearrangement is the Claisen rearrangement. Also see the divinylcyclopropane-cycloheptadiene rearrangement.


  1. ^ Arthur C. Cope; et al.; J. Am. Chem. Soc. 1940, 62, 441.
  2. ^ Rhoads, S. J.; Raulins, N. R.; Org. React. 1975, 22, 1–252. (Review)
  3. ^ Hill, R. K.; Compr. Org. Synth. 1991, 5, 785–826.
  4. ^ Wilson, S. R.; Org. React. 1993, 43, 93–250. (Review)
  5. ^ Michael B. Smith & Jerry March: March's Advanced Organic Chemistry, pp. 1659-1673. John Wiley & Sons, 2007. ISBN 978-0-471-72091-1.
  6. ^ Williams, R. V., Chem. Rev. 2001, 101 (5), 1185–1204.
  7. ^ A Synthesis of Ketones by the Thermal Isomerization of 3-Hydroxy-1,5-hexadienes. The Oxy-Cope Rearrangement Jerome A. Berson, Maitland Jones, , Jr. J. Am. Chem. Soc. 1964; 86(22); 5019–5020. doi:10.1021/ja01076a067
  8. ^ Stepwise Mechanisms in the Oxy-Cope Rearrangement Jerome A. Berson and Maitland Jones pp 5017 – 5018; J. Am. Chem. Soc. 1964; doi:10.1021/ja01076a066
  9. ^ Evans, D.A.; Golob, A.M. J. Am. Chem. Soc. 1975, 97, 4765–4766. doi:10.1021/ja00849a054
  10. ^ Schreiber, S.L.; Santini, S. J. Am. Chem. Soc. 1984, 106, 4038–4039. doi:10.1021/ja00326a028