Iron-Catalyzed S-Arylation of Benzothiazole with Aryl Iodides under Aqueous Medium: Facile Synthesis of Aryl(2-aminoaryl) Sulfides

Hang Wai Lee; Ka Fu Yung; Fuk Yee Kwong

doi:10.1055/s-0034-1379484

Iron-Catalyzed S-Arylation of Benzothiazole with Aryl Iodides under Aqueous Medium: Facile Synthesis of Aryl(2-aminoaryl) Sulfides

Hang Wai Lee, Ka Fu Yung, Fuk Yee Kwong

Research output: Journal article publication › Journal article › Academic research › peer-review

4 Citations (Scopus)

Abstract

A simple route for facile access of aryl(2-aminoaryl) sulfide was reported. With the aid of iron(III) chloride catalyst and diamine ligand, benzothiazole was efficiently S-arylated with various aryl iodides (19 examples) in water under air atmosphere. This operationally simple protocol provides aryl(2-aminoaryl) sulfides in moderate to good yields.

Original language	English
Article number	st-2014-w0764-c
Pages (from-to)	2743-2747
Number of pages	5
Journal	Synlett
Volume	25
Issue number	19
DOIs	https://doi.org/10.1055/s-0034-1379484
Publication status	Published - 1 Dec 2014

Keywords

benzothiazole
catalysis
iron
S-arylation
water

ASJC Scopus subject areas

Organic Chemistry

More information

10.1055/s-0034-1379484

Cite this

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KW - benzothiazole

KW - catalysis

KW - iron

KW - S-arylation

KW - water

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Iron-Catalyzed S-Arylation of Benzothiazole with Aryl Iodides under Aqueous Medium: Facile Synthesis of Aryl(2-aminoaryl) Sulfides

Abstract

Keywords

ASJC Scopus subject areas

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