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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1850873Erstellt: 25. Oktober 2026

O-Methyltyramine → 1-(4-chlorophenyl)-N-[2-(4-methoxyphenyl)ethyl]cyclopropanecarboxamide

https://huagongshe.com/reaction/1850873

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktO-MethyltyramineHCID 4657—
Edukt1-(p-Chlorophenyl)cyclopropanecarboxylic acidHCID 98606—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
LösungsmittelWaterHCID 962—
Produkt1-(4-chlorophenyl)-N-[2-(4-methoxyphenyl)ethyl]cyclopropanecarboxamideHCID 60409668—

Reaktionsschritte

A solution of 1-(4-chlorophenyl)cyclopropanecarboxylic acid (5.0 g, 25.3 mmol), 2-(4-methoxyphenyl)ethanamine (4.2 g, 28 mmol) and 4-N,N-Dimethylaminopyridin (3.3 g; 28 mmol) in methylenehloride (200 ml) was cooled to −10° C. N-ethyl-N′-(3-Dimethylaminopropyl)-carbodiimid hydrochloride (EDC, 5.3 g, 28 mmol) was added in several portions and the resulting mixture stirred overnight. The reaction mixture was poured into water and consecutively extracted with water, 2N NaOH and 1N HCl. Evaporation of the dried (NaSO4) extract yielded an oily residue that crystallized upon addition of n-heptan, which was used without further purification. Yield 7.0 g (21.2 mmol, 83%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08957089B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-bef0d4a902b649ad986996cdb96c4d6a
Quellennotizuspto-grants-2015_02