Organic reactions in ionic liquids: A new method for the synthesis of alkyl aryl sulfones by alkylation of sodium arenesulfinates with unactivated alkyl chlorides

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

doi:10.1081/SCC-200034831

Organic reactions in ionic liquids: A new method for the synthesis of alkyl aryl sulfones by alkylation of sodium arenesulfinates with unactivated alkyl chlorides

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

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

Abstract

A new method is reported for the synthesis of alkyl aryl sulfones by alkylation of sodium arenesulfinates with unactivated alkyl chlorides using ionic liquid based on 1-butyl-3-methylimidazolium tetrafluoroborate (BmimBF ₄) mixed with water (2:1) as reaction media. The ionic liquid can be reused and the procedure gives the sulfones in moderate yields.

Original language	English
Pages (from-to)	4031-4035
Number of pages	5
Journal	Synthetic communications
Volume	34
Issue number	21
DOIs	https://doi.org/10.1081/SCC-200034831
Publication status	Published - 16 Nov 2004

Keywords

alkylation
alkylchlorides
arenesulfinates
ionic liquids
sulfones

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10.1081/SCC-200034831

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abstract = "A new method is reported for the synthesis of alkyl aryl sulfones by alkylation of sodium arenesulfinates with unactivated alkyl chlorides using ionic liquid based on 1-butyl-3-methylimidazolium tetrafluoroborate (BmimBF 4) mixed with water (2:1) as reaction media. The ionic liquid can be reused and the procedure gives the sulfones in moderate yields.",

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

year = "2004",

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TY - JOUR

T1 - Organic reactions in ionic liquids

T2 - A new method for the synthesis of alkyl aryl sulfones by alkylation of sodium arenesulfinates with unactivated alkyl chlorides

AU - Hu, Yi

AU - Chen, Zhen-Chu

AU - Le, Zhang-Gao

AU - Zheng, Qinguo

PY - 2004/11/16

Y1 - 2004/11/16

N2 - A new method is reported for the synthesis of alkyl aryl sulfones by alkylation of sodium arenesulfinates with unactivated alkyl chlorides using ionic liquid based on 1-butyl-3-methylimidazolium tetrafluoroborate (BmimBF 4) mixed with water (2:1) as reaction media. The ionic liquid can be reused and the procedure gives the sulfones in moderate yields.

AB - A new method is reported for the synthesis of alkyl aryl sulfones by alkylation of sodium arenesulfinates with unactivated alkyl chlorides using ionic liquid based on 1-butyl-3-methylimidazolium tetrafluoroborate (BmimBF 4) mixed with water (2:1) as reaction media. The ionic liquid can be reused and the procedure gives the sulfones in moderate yields.

KW - alkylation

KW - alkylchlorides

KW - arenesulfinates

KW - ionic liquids

KW - sulfones

UR - http://www.scopus.com/inward/record.url?scp=7644238620&partnerID=8YFLogxK

UR - https://www.tandfonline.com/doi/abs/10.1081/SCC-200034831

U2 - 10.1081/SCC-200034831

DO - 10.1081/SCC-200034831

M3 - Article

SN - 0039-7911

VL - 34

SP - 4031

EP - 4035

JO - Synthetic communications

JF - Synthetic communications

IS - 21

ER -

Organic reactions in ionic liquids: A new method for the synthesis of alkyl aryl sulfones by alkylation of sodium arenesulfinates with unactivated alkyl chlorides

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