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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1182748생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1182748

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 997217082.7%

반응 조건

온도70 °C

반응 단계

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 4′-methylbiphenyl-2-sulfonic acid 1-dimethylaminometh-(E)-ylideneamide (4.6 g) as a light brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08664227B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-1fc2bc3ca0544779bb2fa9f3c103c5a4
출처 메모uspto-grants-2014_03