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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 529648Erstellt: 25. Oktober 2026

Triethylamine → 4-Amino-3-chloro-N,N-dimethylbenzamide

https://huagongshe.com/reaction/529648

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktDimethylamine, hydrochlorideHCID 10473—
Edukt4-Amino-3-chlorobenzoic acidHCID 17211—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
LösungsmittelIsopropanolHCID 3776—
LösungsmittelChloroformHCID 6212—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Amino-3-chloro-N,N-dimethylbenzamideHCID 2028748159,6%

Reaktionsschritte

To a solution of 4-amino-3-chloro-benzoic acid (1 equiv) in DCM (0.12 M) was added N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (1.2 equiv), 1-hydroxybenzotriazole (1.2 equiv), triethylamine (4 equiv) and dimethylamine hydrochloride (2 equiv) sequentially. The mixture was stirred at room temperature overnight. After the reaction was complete, as monitored by LCMS, the mixture was diluted with a mixture of isopropanol in chloroform (30%,), washed with water and dried over anhydrous sodium sulfate. The organic phase was concentrated and the residue obtained was recrystallized in the mixture of hexane and ethyl acetate (10%,) to afford the desired product (Yield: 59.6%) as a light brown solid. MS (ESI) m/z 199.1 [M+1]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09346812B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-0187656467444a3f8b52cea66baa6d74
Quellennotizuspto-grants-2016_05