Trisha Shetty (Editor)

Chlorosulfonyl isocyanate

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Formula
  
CNClO3S

Density
  
1.63 g/cm³

Boiling point
  
107 °C

Molar mass
  
141.53 g/mol

Melting point
  
-44 °C

Appearance
  
colorless liquid

Chlorosulfonyl isocyanate httpsuploadwikimediaorgwikipediacommonsthu

Related compounds
  
Thionyl chloride Cyanogen bromide Phosphoryl chloride

Chlorosulfonyl isocyanate is the chemical compound ClSO2NCO, known as CSI. This compound is a versatile reagent in organic synthesis.

Contents

Preparation, structure, handling

CSI is prepared by treating cyanogen chloride with sulfur trioxide, the product being distilled directly from the reaction mixture.

In this transformation, both the carbon and the nitrogen termini of CN are functionalized.

The structure of CSI is represented as ClS(O)2-N=C=O. It consists of two electron-withdrawing components, the chlorosulfonyl group (SO2Cl) and the isocyanate group (-N=C=O). Because of its resulting electrophilicity, the use of CSI in chemical synthesis requires relatively inert solvents such as chlorocarbons, acetonitrile, and ethers.

Uses

The molecule has two electrophilic sites, the carbon and the S(VI) center.

CSI has been employed for the preparation of β-lactams, some of which are medicinally important. Thus, alkenes undergo a [2+2]-cycloaddition to give the sulfonamide. The SO2Cl group can be removed simply by hydrolysis, leaving the secondary amide. Other reactions of CSI:

  • Cycloaddition to alkynes to give 1,2,3-oxathiazine-2,2-dioxide-6-chlorides.
  • Conversion of primary alcohols to carbamates.
  • Conversion of carboxylic acids and the acid chlorides into nitriles.
  • Preparation of N,N-disubstituted sulfamides, R2NSO2NH2
  • Safety considerations

    CSI is toxic, corrosive and reacts violently with water. It cannot be stored in glass-stoppered flasks, requiring instead polyethylene bottles.

    References

    Chlorosulfonyl isocyanate Wikipedia


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