Dimethylthiocarbamoyl chloride
Dimethylthiocarbamoyl chloride is an organosulfur compound with the formula (CH3)2NC(S)Cl. A yellow solid, it is often encountered as a yellow syrup. It is a key reagent in the synthesis of arylthiols via the Newman-Kwart rearrangement.[1]
 | |
| Identifiers | |
|---|---|
PubChem CID |
|
| Properties | |
| C3H6ClNS | |
| Molar mass | 123.60 g·mol−1 |
| Appearance | yellow solid |
| Melting point | 39–43 °C (102–109 °F; 312–316 K) |
| Boiling point | 90–95 °C (194–203 °F; 363–368 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Synthesis and reactions
Representative of other thiocarbamoyl chlorides, dimethylthiocarbamoyl chloride is electrophilic, serving as a source of R2NC(S)+.[2] It is analogous to dimethylcarbamoyl chloride (R2NC(O)Cl).
Dimethylthiocarbamoyl chloride is prepared by chlorination of the related tetramethylthiuram disulfide:
- [Me2NC(S)]2S2 + 3 Cl2 → 2 Me2NC(S)Cl + 2 SCl2
Dimethylthiocarbamoyl chloride reacts with dithiocarbamates (R2NCS−
2) to give thiuram sulfides [R2NC(S)]2S. With methanethiolate, it gives methyl dimethyldithiocarbamate (Me2NC(S)SMe).
gollark: Add more turrets then.
gollark: It's still not enough.
gollark: Oh, you need more iron. Of course you do.
gollark: Make more iron gears.
gollark: There is no situation in which this would be beneficial, except something incredibly contrived like some of the power poles being missing but the boilers and inserters still working.
References
- Melvin S. Newman, Frederick W. Hetzel (1971). "Thiophenols from Phenols: 2-Naphthalenethiol". Org. Synth. 51: 139. doi:10.15227/orgsyn.051.0139.CS1 maint: uses authors parameter (link)
- R. J. Cremlyn “An Introduction to Organosulfur Chemistry” John Wiley and Sons: Chichester (1996). ISBN 0 471 95512 4
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.