Selenoxide elimination

Selenoxide elimination (also called α-selenation)[1] is a method for the chemical synthesis of alkenes from selenoxides. It is most commonly used to synthesize α,β-unsaturated carbonyl compounds from the corresponding saturated analogues.[2]

Introduction

After the development of sulfoxide elimination as an effective method for generating carbon–carbon double bonds,[3] it was discovered that selenoxides undergo a similar process, albeit much more rapidly. Most selenoxides decompose to the corresponding alkenes at temperatures between −50 and 40 °C. Evidence suggests that the elimination is syn; however, epimerization at both carbon and selenium (both of which are stereogenic) may occur during the reaction. As selenoxides can be readily prepared from nucleophilic carbonyl derivatives (enols and enolates),[4] selenoxide elimination has grown into a general method for the preparation of α,β-unsaturated carbonyl compounds.

(1)

Mechanism and stereochemistry

Prevailing mechanism

Elimination of selenoxides takes place through an intramolecular, syn elimination pathway. The carbon–hydrogen and carbon–selenium bonds are co-planar in the transition state.[5]

(2)

The reaction is highly trans-selective when acyclic α-phenylseleno carbonyl compounds are employed. Formation of conjugated double bonds is favored. Endocyclic double bonds tend to predominate over exocyclic ones, unless no syn hydrogen is available in the ring. Selenium in these reactions is almost always stereogenic, and the effect of epimerization at selenium (which is acid-catalyzed and occurs readily) on the elimination reaction is nearly unknown. In one example, separation and warming of selenoxides 1 and 2 revealed that 2 decomposes at 0 °C, while 1, which presumably has more difficulty accessing the necessary syn conformation for elimination, is stable to 5 °C.[6]

(3)

Scope and limitations

Selenylating and oxidizing reagents

α-Selenylation of carbonyl compounds can be accomplished with a variety of reagents, using either electrophilic or nucleophilic selenylating reagents. Usually, simple phenylseleno compounds are used in elimination reactions; although 2-nitrophenylselenides react more quickly, they are more expensive to prepare, and phenylselenides typically react in minutes. Electrophilic selenylating reagents can be used in conjunction with enols, enolates, or enol ethers. Phenylselenating reagents include:

  • Diphenyl diselenide
  • Benzeneselenyl chloride
  • Benzeneselenyl bromide
  • Benzeneselinyl chloride
  • Sodium benzeneselenolate
  • Trimethylsilyl phenyl selenide

The most common oxidizing agent employed is hydrogen peroxide (H2O2).[7] It is sometimes used in excess, to overcome catalytic decomposition of H2O2 by selenium; however, undesired oxidation of starting material has been observed under these conditions. Oxidation of products (via the Baeyer-Villiger reaction, for instance) has also been observed.[8]

(4)

For substrates whose product olefins are sensitive to oxidation, meta-Chloroperoxybenzoic acid (mCPBA) can be employed as an oxidant. It oxidizes selenides below the temperature at which they decompose to alkenes; thus, all oxidant is consumed before elimination begins. Buffering with an amine base is necessary before warming to avoid acid-mediated side reactions.[9]

(5)

Ozone, which gives only dioxygen as a byproduct after oxidation, is used to oxidize selenides when special conditions are required for thermolysis or extreme care is necessary during workup. Quinones can be synthesized from the corresponding cyclic unsaturated carbonyl compounds using this method.[10]

(6)

Substrates

α-Phenylseleno aldehydes, which are usually prepared from the corresponding enol ethers, are usually oxidized with mCPBA or ozone, as hydrogen peroxide causes over-oxidation. α-Phenylseleno ketones can be prepared by kinetically controlled enolate formation and trapping with an electrophilic selenylating reagent such as benzeneselenyl chloride. A second deprotonation, forming a selenium-substituted enolate, allows alkylation or hydroxyalkylation of these substrates.[11]

(7)

Base-sensitive substrates may be selenylated under acid-catalyzed conditions (as enols) using benzeneselenyl chloride. Hydrochloric acid generated during the selenylation of transient enol catalyzes tautomerization.[12]

(8)

The seleno-Pummerer reaction is a significant side reaction that may occur under conditions when acid is present.[13] Protonation of the selenoxide intermediate, followed by elimination of hydroxide and hydrolysis, leads to α-dicarbonyl compounds. The reaction is not a problem for more electron-rich carbonyls—generally, fewer side reactions are observed in eliminations of esters and amides.[13]

(9)

A second significant side reaction in reactions of ketones and aldehydes is selenylation of the intermediate selenoxide. This process leads to elimination products retaining a carbon-selenium bond,[14] and is more difficult to prevent than the seleno-Pummerer reaction. Tertiary selenoxides, which are unable to undergo enolization, do not react further with selenium electrophiles.

(10)

Comparison with other methods

Analogous sulfoxide eliminations are generally harder to implement than selenoxide eliminations. Formation of the carbon–sulfur bond is usually accomplished with highly reactive sulfenyl chlorides, which must be prepared for immediate use. However, sulfoxides are more stable than the corresponding selenoxides, and elimination is usually carried out as a distinct operation. This allows thermolysis conditions to be optimized (although the high temperatures required may cause other thermal processes). In addition, sulfoxides may be carried through multiple synthetic steps before elimination is carried out.[15]

(11)

The combination of silyl enol ethers with palladium(II) acetate (Pd(OAc)2), the Saegusa oxidation, gives enones. However, the reaction requires stoichiometric amounts of Pd(OAc)2 and thus is not amenable to large-scale synthesis.[16] Catalytic variants have been developed.[17]

(12)

For β-dicarbonyl compounds, DDQ can be used as an oxidizing agent in the synthesis of enediones. Additionally, some specialized systems give better yields upon DDQ oxidation.[18]

(13)

Experimental conditions and procedure

Typical conditions

Organoselenium reagents are toxic, and care should be taken to avoid undue exposure. Selenylation should be carried out using benzeneselenyl chloride whenever possible. Oxidation-elimination reactions should be carried out in non-polar solvents to avoid polar side reactions, such as the seleno-Pummerer reaction. Constrained or highly enolizable α-phenylseleno carbonyl compounds should be treated with ozone or mCPBA (rather than hydrogen peroxide) at low temperature to avoid side reactions.

The oxidation-elimination process produces a 1:1 molar ratio of benzeneseleninic acid and diphenyl diselenide. As the former slowly degrades in the presence of hydrogen peroxide, it should be promptly removed from the reaction mixture when the reaction is complete via base extraction. This extract can be treated with a reducing agent such as sodium thiosulfate.

See also

  • Saegusa–Ito oxidation

References

This article was sourced from Creative Commons Attribution-ShareAlike License; additional terms may apply. World Heritage Encyclopedia content is assembled from numerous content providers, Open Access Publishing, and in compliance with The Fair Access to Science and Technology Research Act (FASTR), Wikimedia Foundation, Inc., Public Library of Science, The Encyclopedia of Life, Open Book Publishers (OBP), PubMed, U.S. National Library of Medicine, National Center for Biotechnology Information, U.S. National Library of Medicine, National Institutes of Health (NIH), U.S. Department of Health & Human Services, and USA.gov, which sources content from all federal, state, local, tribal, and territorial government publication portals (.gov, .mil, .edu). Funding for USA.gov and content contributors is made possible from the U.S. Congress, E-Government Act of 2002.
 
Crowd sourced content that is contributed to World Heritage Encyclopedia is peer reviewed and edited by our editorial staff to ensure quality scholarly research articles.
 
By using this site, you agree to the Terms of Use and Privacy Policy. World Heritage Encyclopedia™ is a registered trademark of the World Public Library Association, a non-profit organization.