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HRID 71656作成日:2026年10月26日

Ethanol → N,N-dimethyl-N'-[2-(4-methylphenyl)phenyl]sulfonylmethanimidamide

https://huagongshe.com/reaction/71656

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物TolueneHCID 1140—
反応物Potassium CarbonateHCID 11430—
反応物Tolylboronic acidHCID 79799—
反応物N'-(2-bromophenyl)sulfonyl-N,N-dimethylmethanimidamideHCID 11779014—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物N,N-dimethyl-N'-[2-(4-methylphenyl)phenyl]sulfonylmethanimidamideHCID 997217082.7%

反応条件

温度70 °C

反応手順

2-Bromo-N-[1-dimethylaminometh-(E)-ylidene]-benzenesulfonamide (5.4 g, 18.4 mmol), 4-methylphenylboronic acid (5.0 g, 36.8 mmol) and potassium carbonate (5.1 g, 36.8 mmol) were dissolved in water (19.7 mL, 1090 mmol), EtOH (49.2 mL, 842 mmol) and toluene (98.3 mL, 923 mmol). The resulting mixture was stirred under nitrogen. Tetrakis(triphenylphosphine)palladium(0) (1.4 g, 1.2 mmol) was added. The mixture was heated at 60° C. for 115 minutes, at 70° C. for 30 minutes, then cooled to room temperature. Water (100 mL) and EtOAc (100 mL) were added. The mixture was washed with saturated aqueous NaCl, extracted with EtOAc, dried over MgSO4, filtered, and concentrated to yield a red solid. The product was triturated with 1:1 EtOAc:hexanes, filtered, and rinsed with hexanes to yield a reddish-brown solid. The product was triturated with EtOAc, filtered, and rinsing with EtOAc to yield the title compound (4.6 g) as a light brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822522B2
出典データセットuspto-grants-2014_09
ORD IDord-6c85bf86afcb45e79da0eb702a80753f
出典メモuspto-grants-2014_09