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| Names | |||
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IUPAC name
Carbonothioyl dichloride
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| Other names
Thiophosgene; Thiocarbonyl chloride; Carbonothioic dichloride
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| Identifiers | |||
3D model (
JSmol)
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| ChEBI | |||
| ChemSpider | |||
| ECHA InfoCard | 100.006.675 | ||
PubChem
CID
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| RTECS number |
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| UNII | |||
CompTox Dashboard (
EPA)
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| Properties | |||
| CSCl2 | |||
| Molar mass | 114.97 g·mol−1 | ||
| Appearance | Red liquid | ||
| Odor | Persistent, choking odor | ||
| Density | 1.50 g/cm3 | ||
| Boiling point | 70 to 75 °C (158 to 167 °F; 343 to 348 K) | ||
| Decomposes | |||
| Solubility in other solvents | Reacts with amines and alcohols, soluble in polar organic solvents | ||
| -50.6·10−6 cm3/mol | |||
Refractive index (nD)
|
1.558 | ||
| Structure | |||
| planar, sp2, C2v | |||
| Hazards | |||
| Occupational safety and health (OHS/OSH): | |||
Main hazards
|
Highly toxic | ||
| Flash point | 62 °C (144 °F; 335 K) | ||
| Related compounds | |||
Related compounds
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Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |||
Thiophosgene is a red liquid with the formula CSCl2. It is a molecule with trigonal planar geometry. There are two reactive C–Cl bonds that allow it to be used in diverse organic syntheses. [1]
CSCl2 is prepared in a two-step process from carbon disulfide. In the first step, carbon disulfide is chlorinated to give trichloromethanesulfenyl chloride (CCl3SCl), a rare sulfenyl chloride:
- CS2 + 3 Cl2 → CCl3SCl + S2Cl2
The chlorination must be controlled as excess chlorine converts trichloromethanesulfenyl chloride into carbon tetrachloride. Steam distillation separates the trichloromethanesulfenyl chloride and hydrolyzes the disulfur dichloride. Reduction of trichloromethanesulfenyl chloride with, e.g., tin [2] or dihydroanthracene [3] produces thiophosgene:
- CCl3SCl + M → CSCl2 + MCl2
CSCl2 is mainly used to prepare compounds with the connectivity CSX2 where X = OR, NHR. [4] Such reactions proceed via intermediate such as CSClX. Under certain conditions, one can convert primary amines into isothiocyanates. CSCl2 also serves as a dienophile to give, after reduction 5-thiacyclohexene derivatives. Thiophosgene is also known as the appropriate reagent in Corey-Winter synthesis for stereospecific conversion of 1,2-diols into alkenes. [5]
It forms a head-to-tail dimer upon irradiation with UV light: [6]
- 2 CSCl2 → S2(CCl2)2
Unlike thiophosgene monomer, a red liquid, the photodimer, an example of a 1,3- dithietane, is a colourless solid.
Thisphosgene decomposes at 200 °C or above to form carbon disulfide and carbon tetrachloride. [7] It has also been observed decomposing to hydrogen sulfide, hydrogen chloride, and carbonyl sulfide gases via contact with human tissue. [8][ failed verification]
CSCl2 is considered highly toxic. Inhalation of the substance can cause irritation of respiratory system, burns, delayed pulmonary edema and death. [9]
- ^ Manchiu D. S. Lay, Mitchell W. Sauerhoff And Donald R. Saunders "Carbon Disulfide" in Ullmann's Encyclopedia Of Industrial Chemistry, 2000, Wiley-VCH, Weinheim. doi: 10.1002/14356007.a05_185
- ^ Dyson, G. M. (1926). "Thiophosgene". Organic Syntheses. 6: 86. doi: 10.15227/orgsyn.006.0086.
- ^ K. T. Potts, C. Sapino (1972). "Thiocarbonyl halides". In S. Patai (ed.). Acyl Halides. PATAI'S Chemistry of Functional Groups. pp. 349–380. doi: 10.1002/9780470771273.ch11. ISBN 978-0-470-77127-3.
- ^ Pascual, Roxana Martinez "Thiophosgene" Synlett 2015, vol. 26, pp. 1776-1777. doi: 10.1055/s-0034-1380659
- ^ Sharma, S. (1978). "Thiophosgene in Organic Synthesis". Synthesis. 1978 (11): 803–820. doi: 10.1055/s-1978-24896.
- ^ B. Krebs H. Beyer (1969). "Die Kristall- und Molekelstruktur des dimeren Thiophosgens". Z. Anorg. Allg. Chem. 365 (3–4): 199–210. doi: 10.1002/zaac.19693650315.
- ^ U.S. Coast Guard, Department of Transportation (1999). CHRIS - Hazardous Chemical Data. Commandant Instruction 16465.12C. Washington, D.C.: U.S. Government Printing Office — via Cameo Chemicals. As cited in "Thiophosgene" PubChem compound record.
- ^ "Thiophosgene".
- ^ US National Library of Medicine (2020). Hazardous Substances Databank entry, as summarized on "Thiophosgene" PubChem compound record.
- Holleman, Arnold Frederik; Wiberg, Egon (2001), Wiberg, Nils (ed.), Inorganic Chemistry, translated by Eagleson, Mary; Brewer, William, San Diego/Berlin: Academic Press/De Gruyter, ISBN 0-12-352651-5
| Authority control databases: National |
|---|
| |||
|
| |||
| Names | |||
|---|---|---|---|
|
IUPAC name
Carbonothioyl dichloride
| |||
| Other names
Thiophosgene; Thiocarbonyl chloride; Carbonothioic dichloride
| |||
| Identifiers | |||
3D model (
JSmol)
|
|||
| ChEBI | |||
| ChemSpider | |||
| ECHA InfoCard | 100.006.675 | ||
PubChem
CID
|
|||
| RTECS number |
| ||
| UNII | |||
CompTox Dashboard (
EPA)
|
|||
| |||
| |||
| Properties | |||
| CSCl2 | |||
| Molar mass | 114.97 g·mol−1 | ||
| Appearance | Red liquid | ||
| Odor | Persistent, choking odor | ||
| Density | 1.50 g/cm3 | ||
| Boiling point | 70 to 75 °C (158 to 167 °F; 343 to 348 K) | ||
| Decomposes | |||
| Solubility in other solvents | Reacts with amines and alcohols, soluble in polar organic solvents | ||
| -50.6·10−6 cm3/mol | |||
Refractive index (nD)
|
1.558 | ||
| Structure | |||
| planar, sp2, C2v | |||
| Hazards | |||
| Occupational safety and health (OHS/OSH): | |||
Main hazards
|
Highly toxic | ||
| Flash point | 62 °C (144 °F; 335 K) | ||
| Related compounds | |||
Related compounds
|
|||
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |||
Thiophosgene is a red liquid with the formula CSCl2. It is a molecule with trigonal planar geometry. There are two reactive C–Cl bonds that allow it to be used in diverse organic syntheses. [1]
CSCl2 is prepared in a two-step process from carbon disulfide. In the first step, carbon disulfide is chlorinated to give trichloromethanesulfenyl chloride (CCl3SCl), a rare sulfenyl chloride:
- CS2 + 3 Cl2 → CCl3SCl + S2Cl2
The chlorination must be controlled as excess chlorine converts trichloromethanesulfenyl chloride into carbon tetrachloride. Steam distillation separates the trichloromethanesulfenyl chloride and hydrolyzes the disulfur dichloride. Reduction of trichloromethanesulfenyl chloride with, e.g., tin [2] or dihydroanthracene [3] produces thiophosgene:
- CCl3SCl + M → CSCl2 + MCl2
CSCl2 is mainly used to prepare compounds with the connectivity CSX2 where X = OR, NHR. [4] Such reactions proceed via intermediate such as CSClX. Under certain conditions, one can convert primary amines into isothiocyanates. CSCl2 also serves as a dienophile to give, after reduction 5-thiacyclohexene derivatives. Thiophosgene is also known as the appropriate reagent in Corey-Winter synthesis for stereospecific conversion of 1,2-diols into alkenes. [5]
It forms a head-to-tail dimer upon irradiation with UV light: [6]
- 2 CSCl2 → S2(CCl2)2
Unlike thiophosgene monomer, a red liquid, the photodimer, an example of a 1,3- dithietane, is a colourless solid.
Thisphosgene decomposes at 200 °C or above to form carbon disulfide and carbon tetrachloride. [7] It has also been observed decomposing to hydrogen sulfide, hydrogen chloride, and carbonyl sulfide gases via contact with human tissue. [8][ failed verification]
CSCl2 is considered highly toxic. Inhalation of the substance can cause irritation of respiratory system, burns, delayed pulmonary edema and death. [9]
- ^ Manchiu D. S. Lay, Mitchell W. Sauerhoff And Donald R. Saunders "Carbon Disulfide" in Ullmann's Encyclopedia Of Industrial Chemistry, 2000, Wiley-VCH, Weinheim. doi: 10.1002/14356007.a05_185
- ^ Dyson, G. M. (1926). "Thiophosgene". Organic Syntheses. 6: 86. doi: 10.15227/orgsyn.006.0086.
- ^ K. T. Potts, C. Sapino (1972). "Thiocarbonyl halides". In S. Patai (ed.). Acyl Halides. PATAI'S Chemistry of Functional Groups. pp. 349–380. doi: 10.1002/9780470771273.ch11. ISBN 978-0-470-77127-3.
- ^ Pascual, Roxana Martinez "Thiophosgene" Synlett 2015, vol. 26, pp. 1776-1777. doi: 10.1055/s-0034-1380659
- ^ Sharma, S. (1978). "Thiophosgene in Organic Synthesis". Synthesis. 1978 (11): 803–820. doi: 10.1055/s-1978-24896.
- ^ B. Krebs H. Beyer (1969). "Die Kristall- und Molekelstruktur des dimeren Thiophosgens". Z. Anorg. Allg. Chem. 365 (3–4): 199–210. doi: 10.1002/zaac.19693650315.
- ^ U.S. Coast Guard, Department of Transportation (1999). CHRIS - Hazardous Chemical Data. Commandant Instruction 16465.12C. Washington, D.C.: U.S. Government Printing Office — via Cameo Chemicals. As cited in "Thiophosgene" PubChem compound record.
- ^ "Thiophosgene".
- ^ US National Library of Medicine (2020). Hazardous Substances Databank entry, as summarized on "Thiophosgene" PubChem compound record.
- Holleman, Arnold Frederik; Wiberg, Egon (2001), Wiberg, Nils (ed.), Inorganic Chemistry, translated by Eagleson, Mary; Brewer, William, San Diego/Berlin: Academic Press/De Gruyter, ISBN 0-12-352651-5
| Authority control databases: National |
|---|