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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 261899Erstellt: 26. Oktober 2026

Potassium Hydroxide → 4-choro-N-[4-(diethylamino)-1-methylbutyl]-2-nitrobenzamide

https://huagongshe.com/reaction/261899

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
EduktNovoldiamineHCID 78953—
Edukt4-Chloro-2-nitrobenzoyl chlorideHCID 10867784—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelWaterHCID 962—
Produkt4-choro-N-[4-(diethylamino)-1-methylbutyl]-2-nitrobenzamideHCID 13101051—

Reaktionsschritte

To a vigorously stirred mixture containing 970 g. (6.2 moles) of freshly distilled N1,N1 -diethyl-1,4 pentanediamine, 4 l. of 1,2-dichloroethane and 1 l. of water at 5°-10° C. there was simultaneously added dropwise a solution containing 5.95 moles of 4-chloro-2-nitrobenzoyl chloride in approximately 8 l. of 1,2-dichloroethane and a solution containing 410 g. (6.2 moles) of 85% potassium hydroxide in 1 l. of water. When the addition was complete the ice bath was removed and stirring was continued 0.5 hours at room temperature. The organic layer was separated, dried over anhydrous calcium sulfate and evaporated to dryness under vacuum. The residue was dissolved in 3 l. or 1,2-dichloroethane and the resulting solution was treated with decolorizing carbon and filtered. The filtrate was diluted to 6 l. with additional 1,2-dichloroethane to give a pale yellow solution of 4-choro-N-[4-(diethylamino)-1-methylbutyl]-2-nitrobenzamide which was divided into three equal portions which were used directly in the next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04152518
Quelldatensatzuspto-grants-1979_05
ORD IDord-d83532fc3e954dd1be6dfdee0defb5ab
Quellennotizuspto-grants-1979_05