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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 548959Erstellt: 24. Oktober 2026

Dichloromethane → (RS)-S-Methyl-S-(4-nitrophenyl)-N-[(4-chloro-3-pyridyl)sulphonyl]sulphimide

https://huagongshe.com/de/reaction/548959

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt4-Nitrophenyl methyl sulfideHCID 96109—
EduktMagnesium monoxideHCID 6850729—
Edukt5-Chloropyridine-3-sulfonamideHCID 54594706—
EduktAcetic acid;iodosylbenzeneHCID 73357407—
KatalysatorDirhodium tetraacetateHCID 152122—
Produkt(RS)-S-Methyl-S-(4-nitrophenyl)-N-[(4-chloro-3-pyridyl)sulphonyl]sulphimideHCID 5968317346%

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, 683 mg (3.55 mmol) of 5-chloro-3-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). 294 mg (0.82 mmol; yield: 46%) of the product are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07943629B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-5c9938856bf541adb341dac74ee22871
Quellennotizuspto-grants-2011_05