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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 476303생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/476303

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물TolueneHCID 1140—
반응물Potassium CarbonateHCID 11430—
반응물Tolylboronic acidHCID 79799—
반응물N'-(2-bromophenyl)sulfonyl-N,N-dimethylmethanimidamideHCID 11779014—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물N,N-dimethyl-N'-[2-(4-methylphenyl)phenyl]sulfonylmethanimidamideHCID 9972170—

반응 조건

온도60 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637676B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-4b612d6875a444cf807f683c28bc8e10
출처 메모uspto-grants-2014_01