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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1635802Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1635802

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktThionyl ChlorideHCID 24386—
EduktN,N-DimethylethylenediamineHCID 66053—
Edukt2-Iodo-5-nitrobenzoic acidHCID 3848745—
Eduktdichloromethane N,N-dimethylformamideHCID 22350042—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTriethylamineHCID 8471—
Produkt(N,N-Dimethylaminoethyl)-2-Iodo-5-Nitro-BenzamideHCID 6954048970%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06511988B2
Quelldatensatzuspto-grants-2003_01
ORD IDord-167424755fa9415ab139ceb53c356508
Quellennotizuspto-grants-2003_01