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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1976076생성일: 2026년 10월 26일

Sodium Hydroxide → (N,N-Dimethylaminoethyl)-2-Iodo-5-Nitro-Benzamide

https://huagongshe.com/reaction/1976076

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Thionyl ChlorideHCID 24386—
반응물N,N-DimethylethylenediamineHCID 66053—
반응물2-Iodo-5-nitrobenzoic acidHCID 3848745—
반응물dichloromethane N,N-dimethylformamideHCID 22350042—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물(N,N-Dimethylaminoethyl)-2-Iodo-5-Nitro-BenzamideHCID 6954048970%

반응 단계

2-iodo-5-nitro-benzoic acid (3 mmoles) was dissolved in a solution of dry dichloromethane-DMF mixture (v/v 4:1, 5 ml). To the ice-cold solution, was added 6 mmoles of thionyl chloride. The reaction mixture was stirred at room temperature for two hours. The solvent was then evaporated using a rotory evaporator. The residue was dried under vacuum at 50° C. for 30 minutes. The residue was dissolved in dry dichlormethane (5 ml) without any purification. The solution was then cooled to 0° C. To this solution, triethylamine (1 ml) and a solution of N,N-dimethylethylenediamine (3 mmole) in dichloromethane was added. The reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, the reaction mixture was poured into water and basified to pH 12 using 2M NaOH. The organic layer was separated and washed with water, dried over anhydrous magnesium sulfate and concentrated. The (N,N-dimethylaminoethyl)-2-iodo-5-nitro-benzamide compound was separated by silica gel chromatography. The yield was 70%. The melting point was 126-128° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06225323B1
출처 데이터셋uspto-grants-2001_05
ORD IDord-592a3d29d46745a49084b99f74649400
출처 메모uspto-grants-2001_05