Dimethylthiocarbamoyl chloride
Appearance
(Redirected from Thiocarbamoyl chloride)
Names | |
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Preferred IUPAC name
Dimethylcarbamothioyl chloride | |
Identifiers | |
3D model (JSmol)
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PubChem CID
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UNII | |
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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) |
Hazards | |
GHS labelling:[1] | |
Warning | |
H290, H302, H314, H317 | |
P234, P260, P261, P264, P264+P265, P270, P272, P280, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P321, P330, P333+P317, P362+P364, P363, P390, P405, P406, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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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]
Synthesis and reactions
[edit]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).
References
[edit]- ^ Melvin S. Newman; Frederick W. Hetzel (1971). "Thiophenols from Phenols: 2-Naphthalenethiol". Org. Synth. 51: 139. doi:10.15227/orgsyn.051.0139.
- ^ R. J. Cremlyn "An Introduction to Organosulfur Chemistry" John Wiley and Sons: Chichester (1996). ISBN 0 471 95512 4