4-Methyl-N-(phenyl-λ³-iodaneylidene)benzenesulfonamide

• PhINTs [T3967]
• Methyl Phenyl Sulfoxide [M1148]
• Copper(II) Trifluoromethanesulfonate [T1292]
• Acetonitrile

To a solution of copper(II) trifluoromethanesulfonate (52 mg, 0.14 mmol) in acetonitrile (10 mL) was successively added methyl phenyl sulfoxide (0.20 g, 1.4 mmol) and PhINTs (0.59 g, 1.6 mmol) at room temperature under nitrogen atmosphere. The reaction mixture was stirred for 5 hours, then the solvent was removed under reduced pressure. The crude mixture was purified by column chromatography (ethyl acetate:hexane = 1:2 on silica gel), giving compound 1 as a white powder (0.31 g, 70% yield).

The reaction mixture was monitored by ¹H NMR (DMSO-d₆).
PhINTs must be kept cool and be avoided contact with some of organic solvents (ex. THF) due to its high reactivity.

¹H NMR (400 MHz, CDCl₃); δ 8.02 (d, 2H, J = 7.3 Hz), 7.86 (d, 2H, J = 8.2 Hz), 7.71 (t, 1H, J = 7.6 Hz), 7.61 (dd, 2H, J = 7.6, 8.2 Hz), 7.26 (d, 2H, J = 8.2 Hz), 3.43 (s, 3H), 2.40 (s, 3H).

¹³C NMR (101 MHz, CDCl₃); δ 143.0, 140.7, 138.4, 134.5, 129.9, 129.4, 127.6, 126.8, 46.8, 21.7.

• Catalytic Synthesis of Sulfoximines using Copper(II) Salts
• E. Lacôte, M. Amatore, L. Fensterbank, M. Malacria, Synlett 2002, 116.

• [N-(p-Toluenesulfonyl)imino]phenyliodinane
• D. A. Evans, D. A. Barnes, Encyclopedia of Reagents for Organic Synthesis 2001.