Iodomethylation of S-Silylorganyl Mercaptoazole Derivatives with α-Iodoketones

The iodomethylation of 2/3-[dimethyl(phenyl)silylmethylthio]-1,3-benzoimidazoles or -1,2,4-triazole with α-iodoketones of the aliphatic and aromatic series in the absence of basic media and solvents leads to formation of unknown salts based on 2/3-mercaptoazolium cations. Reaction of 2-[dimethyl(phenyl)silylmethylthio]-1,3-benzoxazole with α-iodoketones afforded bis(benzoxazol-2-yl)disulfonium derivatives.

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Publication Details

Journal
Журнал Общей Химии
Published
2024-08-13
DOI
https://doi.org/10.31857/s0044460x24030113
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
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article

Iodomethylation of S-Silylorganyl Mercaptoazole Derivatives with α-Iodoketones

L. V. Zhilitskaya, N. О. Yarosh, И. А. Дорофеев
Журнал Общей Химии
Sulfur-Based Synthesis Techniques
article

Iodomethylation of S-Silylorganyl Mercaptoazole Derivatives with α-Iodoketones

L. V. Zhilitskaya, N. О. Yarosh, И. А. Дорофеев
article en

Abstract

The iodomethylation of 2/3-[dimethyl(phenyl)silylmethylthio]-1,3-benzoimidazoles or -1,2,4-triazole with α-iodoketones of the aliphatic and aromatic series in the absence of basic media and solvents leads to formation of unknown salts based on 2/3-mercaptoazolium cations. Reaction of 2-[dimethyl(phenyl)silylmethylthio]-1,3-benzoxazole with α-iodoketones afforded bis(benzoxazol-2-yl)disulfonium derivatives.

Журнал Общей ХимииVol. 94(3)
A.E. Favorsky Irkutsk Institute of Chemistry (RU)
Clean water and sanitation
Openalex Percentile: Top 91%
Sulfur-Based Synthesis Techniques
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