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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 56237생성일: 2026년 10월 24일

Diiodomethane → 3-((6-nitro-1H-indol-1-yl)methoxy)benzonitrile

https://huagongshe.com/ko/reaction/56237

반응식

참여 물질

역할이름HCID투입량
반응물DiiodomethaneHCID 6346—
반응물3-CyanophenolHCID 13394—
반응물Sodium hydrideHCID 24758—
반응물6-Nitro-1H-indoleHCID 78502—
용매DimethylformamideHCID 6228—
생성물3-((6-nitro-1H-indol-1-yl)methoxy)benzonitrileHCID 9003044751%

반응 단계

To a mixture of NaH (3.0 g, 75.0 mmol, 60%) in DMF (20 mL) were added a solution of 6-nitro-1H-indole (4.86 g, 30.0 mmol) in DMF (10 mL) and a solution of 3-hydroxybenzonitrile (3.57 g, 30.0 mmol) in DMF (10 mL) at 0° C. and the mixture was stirred at rt for 2 h. To the reaction mixture was added a solution of diiodomethane (7.5 mL, 90.0 mmol) in DMF (10 mL) slowly without light and the mixture was stirred at rt for 20 h. The mixture was then quenched with water and filtered. The filtrate was extracted with DCM (30 mL×6) and the combined organic layers were washed with brine (50 mL×3), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:1) to give the title compound as a yellow solid (4.47 g, 51%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434695B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-4ac7af751afe4a0c8814018ded4486d1
출처 메모uspto-grants-2016_09