Jump to content

Dimethylthiocarbamoyl chloride

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Headbomb (talk | contribs) at 18:48, 9 October 2016 (fix minus sign, cleanup sup/sub, replaced: <sup>- → <sup>−, <sub>2</sub><sup>−</sup> → {{su|b=2|p=−}} using AWB). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

General chemical structure of a thiocarbamoyl chloride

A thiocarbamoyl chloride is an organosulfur compound with the formula R2NC(S)Cl (R = alkyl, aryl, etc.).[1] These compounds are electrophiles, serving as a source of R2NC(S)+. They are analogous to carbamoyl chlorides, which have the formula R2NC(O)Cl. A common example of this class of compound is dimethylthiocarbamoyl chloride, Me2NC(S)Cl (CAS#16420-13-6), which is a pale yellow, volatile solid.

Synthesis and reactions

Thiocarbamoyl chlorides are prepared by chlorination of the related thiuram disulfides:

[R2NC(S)]2S2 + 3 Cl2 → 2 R2NC(S)Cl + 2 SCl2

Thiocarbamoyl chlorides react with dithiocarbamates (R2NCS
2
) to give thiuram sulfides [R2NC(S)]2S.

References

  1. ^ R. J. Cremlyn “An Introduction to Organosulfur Chemistry” John Wiley and Sons: Chichester (1996). ISBN 0 471 95512 4.