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HRID 476303作成日:2026年10月26日

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

https://huagongshe.com/reaction/476303

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 9972170—

反応条件

温度60 °C

反応手順

2-Bromo-N-[1-dimethylaminometh-(E)-ylidene]benzenesulfonamide (5.36 g, 18.4 mmol), 4-methylphenylboronic acid (5.0 g, 36.8 mmol), potassium carbonate (5.1 g, 36.8 mmol), water (19.7 mL, 1090 mmol), EtOH (49.2 mL, 842 mmol) and toluene (98.3 mL, 923 mmol) were combined and the mixture was stirred under nitrogen. Tetrakis(triphenylphosphine)palladium(0) (1.4 g, 1.2 mmol) was then added. The mixture was heated at 60° C. for about 2 hours, then heated at 70° C. for 30 minutes. The mixture was then cooled to room temperature and water (100 mL) and EtOAc (100 mL) were added. The mixture was washed with saturated aqueous NaCl, extracted with EtOAc, dried over MgSO4, filtered through Celite® and concentrated to yield the crude product as a red solid (8.6 g). The solid material was triturated with 1:1 EtOAc:hexanes, filtered, and rinsed with hexanes to yield the crude product as a reddish-brown solid (6.2 g). The solid material was again triturated with EtOAc, filtered, and rinsed with EtOAc to yield 4′-methybiphenyl-2-sulfonic acid 1-dimethylaminometh-(E)-ylideneamide as a light brown solid (4.6 g; 96.2% purity).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08637676B2
出典データセットuspto-grants-2014_01
ORD IDord-4b612d6875a444cf807f683c28bc8e10
出典メモuspto-grants-2014_01