Oxy-Cope rearrangement

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Oxy-Cope rearrangement
Named after Arthur C. Cope
Reaction type Rearrangement reaction
Identifiers
Organic Chemistry Portal cope-rearrangement
RSC ontology ID RXNO:0000029

In

sigmatropic rearrangement.[1][2]

The reaction is highly general: a wide variety of precursors undergo the reorganization predictably and with ease, rendering it a highly useful synthetic tool.

keto-enol tautomerization.[4]

Base accelerates the reaction by 1010-1017, the anionic oxy-Cope rearrangement.[3]

The formation of an enolate renders the reaction irreversible in most cases.[3][4][5]

History

Sigmatropic rearrangements are useful organic synthesis.[5] In an effort to demonstrate the versatility of the Cope rearrangement by demonstrating its tolerance of an alcohol situated at C-3 of a 1,5-diene, Berson and Jones heated a bicyclic diene alcohol in the gas phase to give cis-∆5,6-octalone in fair yield.[1]

The modification is immensely appealing as a result of the two new disparately placed functional groups that lend themselves well to a variety of previously unavailable synthetic manipulations.

The next development occurred in 1975, when Evans and Golob reported the tremendous rate enhancements by base. Their use of potassium hydride in the cation's corresponding crown ether became the default approach for most applications. Indeed, in some cases, anionic assistance is intentionally forgone to accommodate for the production of overly sensitive enolate product. For example, in the following reaction only tar was obtained, a result that the authors attributed to the product's ostensible intolerance to base.[6] The original oxy-Cope modification thus to this day occupies a relevant niche in synthetic chemistry.

Mechanism

Both the neutral and anionic variants of the oxy-Cope rearrangement may occur via either concerted or stepwise radical pathways, although the former mode is generally favored.[7][8] The preferred intermediate is characterized by a chair-like conformation.[9] Chirality transfer is effected by a highly ordered transition state.[4][9] The positioning of the double bonds in the most readily accessible transition state determines the stereochemical course of the reaction[3] A boat transition state is disfavored, but rearrangements occur via this path to an appreciable extent as well, resulting in the production of diastereomeric mixtures.

Steric effects can be significant.[10]

Rearrangements for which a chair transition state is geometrically impossible nonetheless occur. In fact, enolate formation provides enough of a driving force to overcome the energetic barrier associated with both dearomatization and the boat conformer.[11]

The concerted, synchronous pathways presented above generally predominate; it was calculated for anionic oxy-Cope processes that a divide of 17-34 kcal/mol favors heterolysis over homolysis.[12] Several factors may bridge this energetic gap.[9]

The large degree of strain and the presence of a methyl group's bulk favored the (Z)- instead of the expected (E)-cyclooctenone isomer, suggesting that the intermediate is not formed synchronously. Only with fragmentation and subsequent isomerization steps could the observed product be rationalized.[9]

A study on the anionic oxy-Cope rearrangement carried out entirely in the gaseous phase reported that the rate enhancement stems not from solvent interactions, but from those within the structure itself.[13]

Rate enhancement

In general, decreasing the stability of the oxy-Cope or anionic oxy-Cope substrate relative to that of the product results in increased rate of reaction by the principle of ground state destabilization. This desirable outcome is readily achieved in a variety of ways. Ionic interactions between metal and

18-crown-6
to achieve the same end afforded a 180-fold maximum rate acceleration. From the above results it was concluded that rate increases as counterions more poorly approximate point charges—and with the addition of counterion-sequestering species.

The inclusion of more polar solvents and catalytic quantities of phase transfer salts has also been demonstrated to exert the same rate-enhancing effect.[15]

Finally, the relief of ring strain over the course of a rearrangement will drive a reaction more forcibly to completion, thereby increasing its rate.

Scope

Because there exist multiple classes of natural products containing eight-membered rings, the syntheses of which having proved difficult, the anionic oxy-Cope rearrangement has been highlighted as a suitable alternative pathway. Its application here offers great stereochemical control, and its use is far more general than the relatively unsuccessful routes that had been employed before its development.[16]

In spite of possible geometrical constraints, the required unsaturated substrates may contain triple bonds in place of either of the double bonds. Such an alkynol was effectively manipulated in the elegant synthesis of both poitediol and dactylol.[5] These interesting sigmatropic rearrangements can occur either with anionic assistance or under thermal conditions.[17]

Of particular interest is the application of the oxy-Cope to situations in which the immediate product reacts further in a predictable manner to furnish a desired final product. This goal was achieved in the synthesis of the cis-hydroazulenone below, in which the oxy-Cope intermediate was characterized by a stereoelectronic configuration amenable to remote SN displacement.[18]

Further considerations

Potassium hydride, a frequently utilized reagent for the anionic oxy-Cope rearrangement, is occasionally contaminated with trace impurities that have been suggested to destroy the dienolate intermediate, resulting in putative polymerization. Macdonald et al., who documented the occurrence, prescribed pre-treatment with iodine to eliminate any potassium superoxide that may persist within a purchased batch of the material. This simple preparatory step, as they describe in their paper, effects dramatic improvement in both yield and reproducibility of results.[19]

Important side reactions include heterolytic cleavage, in which the homoallylic alcohol decomposes into a carbonyl and an

allylic system.[20]

Suppression of this phenomenon is readily achievable by decreasing the ionic nature of the metal-alkoxide bond. Specifically, the use of more electronegative alkali metals or solvents less amenable to cation solvation generates the desired effect.[21] In keeping with the above discussion, the rate of reaction may be diminished but should not approach an unsatisfactory level.

References

  1. ^
    doi:10.1021/ja01076a067
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  2. doi:10.1021/ja01859a055
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  3. ^
    ISBN 9780470084960
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  4. ^ a b c Kürti, Lázló; Czakó, Barbara (2005). Strategic Applications of Named Reactions in Organic Synthesis. Burlington: Elsevier Inc. p. 325.
  5. ^
    ISBN 0471264180
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  6. doi:10.1021/jo00279a010
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  7. doi:10.1016/S0040-4039(01)85627-6
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  8. doi:10.1021/ja00253a027
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  9. ^
    PMID 14595626
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  10. doi:10.1021/ja00522a056
    .
  11. doi:10.1016/s0040-4039(02)01611-8
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  12. doi:10.1016/S0040-4039(01)85626-4
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  13. doi:10.1021/ja00316a036
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  14. doi:10.1021/ja00849a054
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  15. doi:10.1021/jo00350a062
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  16. doi:10.1021/jo00133a007
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  17. doi:10.1021/ja00711a034
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  18. doi:10.1021/jo00234a029
    .
  19. doi:10.1021/jo00357a035
    .
  20. doi:10.1016/S0040-4039(00)86824-0
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  21. doi:10.1021/ja00475a051
    .
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