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Thermal Alkylation of Trimethylphenacyl Ammonium Bromide with Benzyldimethylphenyl Ammonium Chloride

Author

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  • GH Torosyan

    (National polytechnic university of Armenia, Asia)

Abstract

The alkylating ability of quaternary ammonium salts (Quat) has been known for a long time [1-3]. Alkylation with Quat-s is advantageous both in cases where the alkyl ammonium salt is more accessible than the alkyl halide and in those cases where the alkylated compound is unstable under alkylation conditions by alkyl halides (for example, in alkaline media). Considering this circumstance in this report turned to the almost forgotten method of alkylation of the element-H acids by Quat-s.

Suggested Citation

  • GH Torosyan, 2017. "Thermal Alkylation of Trimethylphenacyl Ammonium Bromide with Benzyldimethylphenyl Ammonium Chloride," Organic & Medicinal Chemistry International Journal, Juniper Publishers Inc., vol. 4(2), pages 22-23, October.
    • Handle: RePEc:adp:jomcij:v:4:y:2017:i:2:p:22-23
    DOI: 10.19080/OMCIJ.2017.04.555631
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