Organic reactions in ionic liquids: An efficient method for selective S-alkylation of 2-mercaptobenzothia(xa)zole with alkyl halides

Yi Hu; Zhen-Chu Chen; Zhang-Gao Le; Qinguo Zheng

doi:10.1081/SCC-120037917

Organic reactions in ionic liquids: An efficient method for selective S-alkylation of 2-mercaptobenzothia(xa)zole with alkyl halides

Yi Hu
, Zhen-Chu Chen
, Zhang-Gao Le
, Qinguo Zheng

Research output: Contribution to journal › Article › peer-review

22 Citations (Scopus)

Abstract

Ionic liquids based on 1-butyl-3-methylimidazolium hexafluorophosphate (BmimPF₆) and 1-butyl-3-methylimidazolium tetrafluoroborate (BmimBF₄) are used as reusable reaction medium in the selective S-alkylation of 2-mercaptobenzothia(xa)zole with alkyl halides in the presence of potassium carbonate. This procedure is convenient, efficient, and generally gives rise to the S-alkylated product exclusively.

Original language	English
Pages (from-to)	2039-2046
Number of pages	8
Journal	Synthetic communications
Volume	34
Issue number	11
DOIs	https://doi.org/10.1081/SCC-120037917
Publication status	Published - 28 Jun 2004

Keywords

2-Mercaptobenzothia(xa)zole
alkyl halides
ionic liquids
organic reaction
S-Alkylation

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10.1081/SCC-120037917

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title = "Organic reactions in ionic liquids: An efficient method for selective S-alkylation of 2-mercaptobenzothia(xa)zole with alkyl halides",

abstract = "Ionic liquids based on 1-butyl-3-methylimidazolium hexafluorophosphate (BmimPF6) and 1-butyl-3-methylimidazolium tetrafluoroborate (BmimBF4) are used as reusable reaction medium in the selective S-alkylation of 2-mercaptobenzothia(xa)zole with alkyl halides in the presence of potassium carbonate. This procedure is convenient, efficient, and generally gives rise to the S-alkylated product exclusively.",

keywords = "2-Mercaptobenzothia(xa)zole, alkyl halides, ionic liquids, organic reaction, S-Alkylation",

author = "Yi Hu and Zhen-Chu Chen and Zhang-Gao Le and Qinguo Zheng",

year = "2004",

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language = "English",

volume = "34",

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T1 - Organic reactions in ionic liquids

T2 - An efficient method for selective S-alkylation of 2-mercaptobenzothia(xa)zole with alkyl halides

AU - Hu, Yi

AU - Chen, Zhen-Chu

AU - Le, Zhang-Gao

AU - Zheng, Qinguo

PY - 2004/6/28

Y1 - 2004/6/28

N2 - Ionic liquids based on 1-butyl-3-methylimidazolium hexafluorophosphate (BmimPF6) and 1-butyl-3-methylimidazolium tetrafluoroborate (BmimBF4) are used as reusable reaction medium in the selective S-alkylation of 2-mercaptobenzothia(xa)zole with alkyl halides in the presence of potassium carbonate. This procedure is convenient, efficient, and generally gives rise to the S-alkylated product exclusively.

AB - Ionic liquids based on 1-butyl-3-methylimidazolium hexafluorophosphate (BmimPF6) and 1-butyl-3-methylimidazolium tetrafluoroborate (BmimBF4) are used as reusable reaction medium in the selective S-alkylation of 2-mercaptobenzothia(xa)zole with alkyl halides in the presence of potassium carbonate. This procedure is convenient, efficient, and generally gives rise to the S-alkylated product exclusively.

KW - 2-Mercaptobenzothia(xa)zole

KW - alkyl halides

KW - ionic liquids

KW - organic reaction

KW - S-Alkylation

UR - https://www.scopus.com/pages/publications/2942677014

UR - https://www.tandfonline.com/doi/abs/10.1081/SCC-120037917

U2 - 10.1081/SCC-120037917

DO - 10.1081/SCC-120037917

M3 - Article

SN - 0039-7911

VL - 34

SP - 2039

EP - 2046

JO - Synthetic communications

JF - Synthetic communications

IS - 11

ER -

Organic reactions in ionic liquids: An efficient method for selective S-alkylation of 2-mercaptobenzothia(xa)zole with alkyl halides

Abstract

Keywords

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