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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 548958Erstellt: 26. Oktober 2026

4-Nitrophenyl methyl sulfide → (RS)-S-Methyl-S-(4-nitrophenyl)-N-[(5-methyl-2-pyridyl)sulphonyl]sulphimide

https://huagongshe.com/reaction/548958

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Nitrophenyl methyl sulfideHCID 96109—
Edukt5-Methyl-2-pyridinesulfonamideHCID 3614199—
EduktMagnesium monoxideHCID 6850729—
EduktAcetic acid;iodosylbenzeneHCID 73357407—
KatalysatorDirhodium tetraacetateHCID 152122—
LösungsmittelDichloromethaneHCID 6344—
Produkt(RS)-S-Methyl-S-(4-nitrophenyl)-N-[(5-methyl-2-pyridyl)sulphonyl]sulphimideHCID 5968315454%

Reaktionsschritte

879 mg (2.73 mmol) of iodosobenzene diacetate are added to a suspension of 300 mg (1.77 mmol) of 1-methylsulphanyl-4-nitrobenzene, 610 mg (3.55 mmol) of 5-methyl-2-pyridinesulphonamide, 285 mg (7.10 mmol) of magnesium oxide and 78 mg (0.18 mmol) of rhodium(II) acetate dimer in 12 ml of dichloromethane at room temperature. The mixture is stirred for 24 h and then concentrated. The resulting residue is purified by chromatography (dichloromethane/ethanol 95:5). 326 mg (0.96 mmol; yield: 54%) of the product are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07943629B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-12623970122e4eeeab7da493dd147b95
Quellennotizuspto-grants-2011_05