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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1169708Erstellt: 24. Oktober 2026

Sodium Thiosulfate → 1-(Methylsulfinyl)-4-nitrobenzene

https://huagongshe.com/de/reaction/1169708

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ThiosulfateHCID 24477—
EduktMetaperiodic acidHCID 65185—
Edukt4-Nitrophenyl methyl sulfideHCID 96109—
KatalysatorIron chloride (FeCl3)HCID 24380—
LösungsmittelAcetonitrileHCID 6342—
Produkt1-(Methylsulfinyl)-4-nitrobenzeneHCID 305882—

Reaktionsschritte

A suspension of 25.00 g (147.8 mmol) 1-methylsulphanyl-4-nitro-benzene and 0.69 g (4.2 mmol) iron(III) chloride (anhydrous) in 120 ml acetonitrile is treated with 36.0 g (158.1 mmol) periodic acid and stirred at room temperature. At the start of heat evolution, the mixture is transiently cooled with an ice-bath, so that the temperature does not rise above 30° C. After the heat evolution has subsided, the mixture is stirred at room temperature for a further 10 mins. The mixture is poured into a solution of 150 g sodium thiosulphate in 1000 ml ice-water and then extracted with DCM. The combined organic phases are washed with saturated NaCl solution, dried (Na2SO4), filtered and concentrated. The remaining residue is recrystallised from toluene. 23.6 g (128.0 mmol, corresponding to 86% of theor.) of the product is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07825128B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-28910b1747254515a0eb5f5d7c5bf943
Quellennotizuspto-grants-2010_11