Issue 4, 2014

A recyclable and base-free method for the synthesis of 3-iodothiophenes by the iodoheterocyclisation of 1-mercapto-3-alkyn-2-ols in ionic liquids

Abstract

The first example of an iodocyclisation reaction made recyclable by the use of an ionic liquid as the reaction medium is reported. Readily available 1-mercapto-3-alkyn-2-ols were smoothly converted into the corresponding 3-iodothiophenes (50–81% yields, 10 examples) when allowed to react with iodine (1–2 equiv.) in a proper ionic liquid, such as 1-ethyl-3-methylimidazolium ethyl sulfate (EmimEtSO4), as the solvent under mild reaction conditions (25 °C) and in the absence of an external base. The reaction medium can be recycled several times without significantly affecting the reaction outcome. Theoretical calculations have also been performed to investigate the role of the ionic liquid anion in the reaction.

Graphical abstract: A recyclable and base-free method for the synthesis of 3-iodothiophenes by the iodoheterocyclisation of 1-mercapto-3-alkyn-2-ols in ionic liquids

Supplementary files

Article information

Article type
Paper
Submitted
23 Sep 2013
Accepted
11 Nov 2013
First published
14 Nov 2013

Org. Biomol. Chem., 2014,12, 651-659

A recyclable and base-free method for the synthesis of 3-iodothiophenes by the iodoheterocyclisation of 1-mercapto-3-alkyn-2-ols in ionic liquids

R. Mancuso, C. S. Pomelli, C. Chiappe, R. C. Larock and B. Gabriele, Org. Biomol. Chem., 2014, 12, 651 DOI: 10.1039/C3OB41928B

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