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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 607344Erstellt: 26. Oktober 2026

Di-p-tolyl sulphide → Methyl phenyl sulfoxide

https://huagongshe.com/reaction/607344

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDi-p-tolyl sulphideHCID 69294—
Edukt2-Iodoxybenzoic acidHCID 108794—
KatalysatorTetraethylammonium BromideHCID 6285—
LösungsmittelChloroform waterHCID 22418719—
ProduktMethyl phenyl sulfoxideHCID 1451699,9%

Reaktionsschritte

To a stirred suspension of iodoxybenzoic acid (3.7 g, 13.2 mmol, 1.1 eq) in 100:1 CHCl3/H2O (25 mL) was added tetraethylammonium bromide (TEAB) (126 mg, 5 mol %), followed by the addition of p-tolyl sulfide (1.66 g, 12 mmol) in one portion. The mixture was stirred at room temperature for approximately 30 minutes until consumption of sulfide was observed (TLC, hexanes/EtOAc 1/1). The residual solids were removed by filtration and washed with CHCl3 (40 mL). The combined filtrate was washed successively with saturated aq. NaHCO3 (30 mL), saturated aq. NaCl (30 mL), dried over sodium sulfate, and concentrated to provide the crude product. Purification by silica gel column chromatography (50% hexanes/EtOAc elution) afforded the title compound (1.68 g, yield 91%). 1H NMR (300 MHz, CDCl3) δ 7.52 (d, J=8.4 Hz, 2H), 7.32 (d, J=8.4 Hz, 2H), 2.71 (s, 3H), 2.42 (s, 3H); ESI-MS m/z 154.7 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07915443B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-dae94bc90b4e40c9bfccf2a358742dc0
Quellennotizuspto-grants-2011_03