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HRID 607344作成日:2026年10月27日

Di-p-tolyl sulphide → Methyl phenyl sulfoxide

https://huagongshe.com/reaction/607344

反応式

関与物質

役割名称HCID仕込み量
反応物Di-p-tolyl sulphideHCID 69294—
反応物2-Iodoxybenzoic acidHCID 108794—
触媒Tetraethylammonium BromideHCID 6285—
溶媒Chloroform waterHCID 22418719—
生成物Methyl phenyl sulfoxideHCID 1451699.9%

反応手順

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)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07915443B2
出典データセットuspto-grants-2011_03
ORD IDord-dae94bc90b4e40c9bfccf2a358742dc0
出典メモuspto-grants-2011_03