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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 649생성일: 2026년 10월 23일

N,N-Dimethylethylenediamine → N-(4-bromo-3-methoxyphenyl)-N',N'-dimethylethane-1,2-diamine

https://huagongshe.com/ko/reaction/649

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylethylenediamineHCID 66053—
반응물1-Bromo-4-iodo-2-methoxybenzeneHCID 12187202—
시약Sodium t-butoxideHCID 23676156—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물N-(4-bromo-3-methoxyphenyl)-N',N'-dimethylethane-1,2-diamineHCID 8286802045.64%

반응 조건

온도80 °C

반응 단계

A solution of 1-bromo-4-iodo-2-methoxybenzene (0.63 g, 2.01 mmol) dissolved in toluene (15.73 ml) was treated with N1,N1-dimethylethane-1,2-diamine (0.177 g, 2.01 mmol), SODIUM TERT-BUTOXIDE (0.232 g, 2.42 mmol), XANTPHOS (0.116 g, 0.20 mmol) and TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (0.046 g, 0.05 mmol) under nitrogen. The resulting mixture was stirred at 80 °C in a sealed tube for 2 hours. The reaction mixture was diluted with water (200 mL), and extracted with ethyl acetate (200 mL). The organic was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution 0-10% methanol in dcm. Pure fractions were evaporated to dryness to afford N1-(4-bromo-3-methoxyphenyl)-N2,N2-dimethylethane-1,2-diamine (0.251 g, 45.6 %) as a brown oil.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-a7c71c7b356644fcbb6f6b90814539ca
출처 메모750 AstraZeneca ELN dataset