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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1632041생성일: 2026년 10월 25일

Ethanol → 3-Iodo-4-methoxyaniline

https://huagongshe.com/reaction/1632041

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물NitrogenHCID 947—
반응물Ammonium ChlorideHCID 25517—
반응물2-Iodo-1-methoxy-4-nitrobenzeneHCID 94806—
촉매IronHCID 23925—
용매WaterHCID 962—
생성물3-Iodo-4-methoxyanilineHCID 2205459688%

반응 조건

온도85 °C

반응 단계

In a 3-neck 250 mL round-bottomed flask equipped with a stir bar, condenser and N2 lines was placed iron powder (3.50 g, 62.7 mmol), ammonium chloride (4.88 g, 91.3 mmol), ethanol (72 mL) and water (23 mL). The mixture was heated to 85° C. and then 2-iodo-1-methoxy-4-nitro-benzene (5.0 g, 17.9 mmol) was added portion wise over a period of about 2 minutes. The mixture was allowed to stir at 85° C. for 2 hours and then filtered through celite. The celite was washed with EtOH (100 mL) and the filtrate was concentrated. To the concentrated material was added water (100 mL) and ethyl acetate (150 mL). The organic portion was removed and the aqueous portion was re-extracted with ethyl acetate (150 mL). The organic portions were combined, washed with brine (150 mL), dried (MgSO4) and concentrated. The crude material was purified by column chromatography utilizing 50% EtOAc/hexanes as the eluent to produce 3.92 g of 3-iodo-4-methoxy-phenylamine (I-45, X═I, Y═H, Z═NH2, R1═CH3) as a brown semi-solid in 88% yield. MS (ESI+): 250.1 (M+1)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08791267B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-4f06cf6bf0854e2e8fc1a18e2f09d0dd
출처 메모uspto-grants-2014_07