Sodium phenoxide

Sodium phenoxide
Names
Other names
Sodium phenolate
Identifiers
139-02-6
ChemSpider 8420
Jmol interactive 3D Image
PubChem 4445035
Properties
C6H5NaO
Molar mass 116.09 g/mol
Appearance White solid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Sodium phenoxide is an organic compound with the formula NaOC6H5. This white solid is the conjugate base of phenol. It is used as a precursor to many other organic compounds, such as aryl ethers.

Synthesis and structure

Most commonly, solutions of sodium phenoxide are produced by treating phenol with sodium hydroxide.[1] Anhydrous derivatives can be prepared from phenol and sodium:

Na + HOC6H5 → NaOC6H5 + 1/2 H2

Like other sodium alkoxides, crystalline sodium phenolate adopts a complex structures involving multiple Na-O bonds. Solvent-free material is polymeric, each Na center being bound to three oxygen ligands as well as the phenyl ring. Adducts of sodium phenoxide are molecular, such as the cubane [NaOPh]4(HMPA)4.[2]

Reactions

Sodium phenoxide is a moderately strong base. At low pH's gives phenol:[3]

PhOH PhO + H+          (K = 10−10)

Sodium phenoxide can be used to prepare phenyl ethers and metal phenolates:[1]

NaOC6H5 + RBr → ROC6H5 + NaBr

References

  1. 1 2 C. S. Marvel and A. L. Tanenbaum "γ-Phenoxypropyl Bromide" Org. Synth. 1929, vol. 9, pp. 72.
  2. Michael Kunert, Eckhard Dinjus, Maria Nauck, Joachim Sieler "Structure and Reactivity of Sodium Phenoxide - Following the Course of the Kolbe-Schmitt Reaction" Chemische Berichte 1997 Volume 130, Issue 10, pages 1461–1465. doi:10.1002/cber.19971301017
  3. Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, ISBN 0-471-72091-7

External links

Media related to Sodium phenoxide at Wikimedia Commons

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