3-(2-aminophenyl)-4-methyl-1,3-thiazole-2(3H)-thione as an ecofriendly sulphur transfer agent to prepare alkanethiols in high yield and high purity.
Mohammed Amine Mehdid, Ayada Djafri, Christian Roussel, Federico Andreoli
Index: Molecules 14(11) , 4634-43, (2009)
Full Text: HTML
Abstract
A new process is described for preparing very pure linear alkanethiols and linear alpha,omega-alkanedithiols using a sequential alkylation of the title compound, followed by a ring closure to quantitatively give the corresponding 3-methyl[1,3]thiazolo[3,2-a]-[3,1]benzimidazol-9-ium salt and the alkanethiol derivative under mild conditions. The alkanethiol and the heteroaromatic salt are easily separated by a simple extraction process. The intermediate thiazolium quaternary salts resulting from the first reaction step can be isolated in quantitative yields, affording an odourless protected form of the thiols.
Related Compounds
Related Articles:
2015-12-01
[J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 1006 , 151-7, (2015)]
Epidithiol formation by an unprecedented twin carbon-sulfur lyase in the gliotoxin pathway.
2012-10-01
[Angew. Chem. Int. Ed. Engl. 51(40) , 10064-8, (2012)]
2015-11-02
[Chemistry 21 , 16035-46, (2015)]
2009-09-15
[Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 74(1) , 67-73, (2009)]
2013-11-15
[J. Mol. Biol. 425(22) , 4366-78, (2013)]