Chlorosulfonyl isocyanate

CSI is prepared by treating cyanogen chloride with sulfur trioxide, the product being distilled directly from the reaction mixture. ::SO3 + ClCN → ClSO2NCO In this transformation, both the carbon and the nitrogen termini of CN are functionalized. The structure of CSI is represented as . It consists of two electron-withdrawing components, the chlorosulfonyl group (SO2Cl) and the isocyanate group (). 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 • Preparation of Burgess reagent ==Safety considerations==

CSI is toxic, corrosive and reacts violently with water. ==Chemical properties==

Chlorosulfonyl isocyanate reacts with sodium monofluoride to form fluorosulfonyl isocyanate: :: ==References==