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HRID 1635802作成日:2026年10月26日

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

https://huagongshe.com/reaction/1635802

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Thionyl ChlorideHCID 24386—
反応物N,N-DimethylethylenediamineHCID 66053—
反応物2-Iodo-5-nitrobenzoic acidHCID 3848745—
反応物dichloromethane N,N-dimethylformamideHCID 22350042—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物(N,N-Dimethylaminoethyl)-2-Iodo-5-Nitro-BenzamideHCID 6954048970%

反応手順

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-nitrobenzamide compound was separated by silica gel chromatography. The yield was 70%. The melting point was 126-128° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06511988B2
出典データセットuspto-grants-2003_01
ORD IDord-167424755fa9415ab139ceb53c356508
出典メモuspto-grants-2003_01