Thermal Alkylation of Trimethylphenacyl Ammonium Bromide with Benzyldimethylphenyl Ammonium Chloride

Torosyan Gh
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Torosyan Gh: National polytechnic university of Armenia, Asia

Organic & Medicinal Chemistry International Journal, 2017, vol. 4, issue 2, 22-23

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.

Keywords: juniper publishers:Medicinal Chemistry; Biochemistry Journal; Pharmacology Journal; biochemical pharmacology; molecular pharmacology; biochemistry; open access journals; peer reviewed journals; Open Access; Journal of Molecular Biochemistry; International Research Journal of Pure and Applied Chemistry; World Journal of Biological Chemistry; Biochemistry and Analytical Biochemistry; Biochemistry & Physiology: Open Access; Molecular Biology International; Plant Biochemistry & Physiology; International Journal of Molecular Sciences; Journal of Clinical and Medical Genomics; Environmental Analytical Chemistry; Medicinal Chemistry; Juniper publishers reivews (search for similar items in EconPapers)
Date: 2017
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Persistent link: https://EconPapers.repec.org/RePEc:adp:jomcij:v:4:y:2017:i:2:p:22-23

DOI: 10.19080/OMCIJ.2017.04.555631

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