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Oxonium ion

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Title: Oxonium ion  
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Subject: Hydronium, Prins reaction, Oxonium, Woodward cis-hydroxylation, Tiffeneau–Demjanov rearrangement
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Oxonium ion

In oxocarbenium ions, obtained by protonation or alkylation of a carbonyl group e.g. R-C=O+-R' which forms a resonance structure with the fully fledged carbocation R-C+-O-R' and is therefore especially stable:

Stable alkyloxonium salts exist; they are extensively used as alkylating agents. For example, triethyloxonium tetrafluoroborate (Et
3
O+
)(BF
4
) is a white crystalline solid. It is a powerful ethylating agent. It can be used, for example, to produce ethyl esters when the conditions of traditional Fischer esterification are unsuitable.[2] It is also used for preparation of enol ethers and related functional groups.[3][4]

general pyramidal
oxonium ion
skeletal formula of the
trimethyloxonium cation
ball-and-stick model
of trimethyloxonium
space-filling model
of trimethyloxonium

Other hydrocarbon oxonium ions are formed by protonation or alkylation of alcohols or ethers (R-C-O+
-R
1
R
2
). In acidic media, the oxonium functional group produced by protonating an alcohol can be a leaving group in the E2 elimination reaction, because when it receives an electron, it becomes a water molecule. The product is an alkene. Extreme acidity, heat and dehydrating conditions are usually required.

Oxatriquinane and oxatriquinacene are unusually stable oxonium ions, first described in 2008. Oxatriquinane does not react with boiling water or with alcohols, thiols, halide ions, or amines, although it does react with stronger nucleophiles such as hydroxide, cyanide, and azide.

See also

References

  1. ^  
  2. ^ Douglas J. Raber, Patrick Gariano, Jr, Albert O. Brod, Anne L. Gariano, And Wayne C. Guida "Esterification Of Carboxylic Acids With Trialkyloxonium Salts: Ethyl And Methyl 4-acetoxybenzoates" Org. Synth. 1977, volume 56, 59.doi:10.15227/orgsyn.056.0059
  3. ^ Justin R. Struble And Jeffrey W. Bode "Synthesis Of A N-mesityl Substituted Aminoindanol-derived Triazolium Salt" Org. Synth. 2010, volume 87, 362. doi:10.15227/orgsyn.087.0362
  4. ^ Lous S. Hegedus, Michael A. Mcguire, And Lisa M. Schultze "1,3-Dimethyl-3-methoxy-4-phenylazetidinone" Org. Synth. 1987, volume 65, 140.doi:10.15227/orgsyn.065.0140
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