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Sulfuryl chloride

Chemical compound From Wikipedia, the free encyclopedia

Sulfuryl chloride
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Sulfuryl chloride is an inorganic compound with the formula SO2Cl2. At room temperature, it is a colorless liquid with a pungent odor. Sulfuryl chloride is not found in nature.

Quick facts Names, Identifiers ...

Sulfuryl chloride is commonly confused with thionyl chloride, SOCl2. The properties of these two sulfur oxychlorides are quite different: sulfuryl chloride is a source of chlorine whereas thionyl chloride is a source of chloride ions. An alternative IUPAC name is sulfuryl dichloride.

Sulfur is tetrahedral in SO2Cl2 and the oxidation state of the sulfur atom is +6, as in sulfuric acid.

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Synthesis

SO2Cl2 is prepared by the reaction of sulfur dioxide and chlorine in the presence of a catalyst, such as activated carbon.[2]

SO2 + Cl2 → SO2Cl2

The product can be purified by fractional distillation.

Legacy routes

Sulfuryl chloride was first prepared in 1838 by the French chemist Henri Victor Regnault.[3]

Older routes include oxidation of thionyl chloride:

5 SOCl2 + HgO → ClSSCl + HgCl2 + 3 SO2Cl2
2 SOCl2 + MnO2 → SO2 + MnCl2 + SO2Cl2
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Reactions

Sulfuryl chloride reacts with water, releasing hydrogen chloride gas and sulfuric acid:

2 H2O + SO2Cl2 → 2 HCl + H2SO4

For sulfuryl chloride, this happens at room temperature, but the related sulfuryl fluoride does not hydrolyse at temperatures up to 150 °C.

SO2Cl2 will also decompose when heated to or above 100 °C, about 30 °C above its boiling point.

Upon standing, SO2Cl2 decomposes to sulfur dioxide and chlorine, which gives the older samples a slightly yellowish color.[2]

SO2Cl2 can be used as a source of chlorine in alkane radical chlorination, initiated chemically (usually by peroxide) or by light:[4]

CH4 + SO2Cl2 → CH3Cl + SO2 + HCl
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Uses

Sulfuryl chloride is used as a source of Cl2. Because it is a pourable liquid, it is considered more convenient than Cl2 to dispense.

Sulfuryl chloride is used in the conversion of C−H to C−Cl adjacent to activating substituents such as carbonyls and sulfoxides:[5][6]

RC(O)CH2R' + SO2Cl2 → RC(O)CHClR' + HCl + SO2

It also chlorinates alkanes, alkenes, alkynes, aromatics, ethers (such as tetrahydrofuran) and epoxides. Such reactions occur under free radical conditions using an initiator such as AIBN. It convert thiols or disulfides into the corresponding sulfenyl chlorides:[7]

RSH + SO2Cl2 → RSCl + HCl + SO2

Occasionally, sulfinyl chlorides result from such reactions.[8] SO2Cl2 can also convert alcohols to alkyl chlorides. In industry, sulfuryl chloride is most used in producing pesticides. Phosphorus pentachloride is prepared by the reaction of white phosphorus with sulfuryl chloride.

Sulfuryl chloride can also be used to treat wool to prevent shrinking.

Precautions

Sulfuryl chloride is toxic, corrosive, and acts as a lachrymator. It releases hydrogen chloride upon contact with water, as well as donor solvents such as dimethyl sulfoxide and dimethylformamide.

References

Further reading

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