Tetraethylammonium chloride

Preparation and structure

TEAC is produced by alkylation of triethylamine with ethyl chloride.

TEAC exists as either of two stable hydrates, the monohydrate and tetrahydrate. The crystal structure of has been determined, as has that of the tetrahydrate, .

Details for the preparation of large, prismatic crystals of are given by Harmon and Gabriele, who carried out IR-spectroscopic studies on this and related compounds. These researchers have also pointed out that, although freshly-purified is free of triethylamine hydrochloride, small quantities of this compound form on heating of TEAC as the result of a Hofmann elimination: :

Synthetic applications

To a large extent, the synthetic applications of TEAC resemble those of tetraethylammonium bromide (TEAB) and tetraethylammonium iodide (TEAI), although one of the salts may be more efficacious than another in a particular reaction. For example, TEAC produces better yields than TEAB or TEAI as a co-catalyst in a reaction to prepare diarylureas from arylamines, nitroaromatics and carbon monoxide.

In other examples, such as the following, TEAC is not as effective as TEAB or TEAI:

• 2-Hydroxyethylation (attachment of ) by ethylene carbonate of carboxylic acids and certain heterocycles bearing an acidic N-H.
• Phase-transfer catalyst in geminal di-alkylation of fluorene, N,N-dialkylation of aniline and N-alkylation of carbazole using aqueous sodium hydroxide and alkyl halides.

Biology

In common with tetraethylammonium bromide and tetraethylammonium iodide, TEAC has been used as a source of tetraethylammonium ions for numerous clinical and pharmacological studies, which are covered in more detail under the entry for Tetraethylammonium. Briefly, TEAC has been explored clinically for its ganglionic blocking properties, although it is now essentially obsolete as a drug, and it is still used in physiological research for its ability to block channels in various tissues.

Toxicity

The toxicity of TEAC is primarily due to the tetraethylammonium ion, which has been studied extensively. The acute toxicity of TEAC is comparable to that of tetraethylammonium bromide and tetraethylammonium iodide. These data are provided for comparative purposes; additional details may be found in the entry for Tetraethylammonium.

References

References

1. ''[[The Merck Index]]'', 10th Ed., p.1316, Rahway: Merck & Co.
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8. T.Yoshino et al. (1977). "Synthetic studies with carbonates. Part 6. Syntheses of 2-hydroxyethyl derivatives by reactions of ethylene carbonate with carboxylic acids or heterocycles in the presence of tetraethylammonium halides or under autocatalytic conditions". ''J. Chem. Soc., Perkin 1'' 1266–1272.
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10. G. K. Moe and W. A. Freyburger (1950). "Ganglionic blocking agents". ''Pharmacol. Rev.'' '''2''' 61–95.
11. B. Hille (1967). "The selective inhibition of delayed potassium currents in nerve by tetraethylammonium ions". ''J. Gen. Physiol.'' '''50''' 1287–1302.
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13. O. M. Gruhzit, R. A. Fisken and B. J. Cooper (1948). "Tetraethylammonium chloride [(C₂H₅)₄NCl]. Acute and chronic toxicity in experimental animals". ''J. Pharmacol. Exp. Ther.'' '''92''' 103–107.