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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36431Erstellt: 25. Oktober 2026

Hydrochloric Acid → N-methyl-2-(2-phenoxyphenyl)-2-oxoacetamide

https://huagongshe.com/reaction/36431

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTriethylamineHCID 8471—
EduktDiphosgeneHCID 10426—
EduktThionyl ChlorideHCID 24386—
EduktN-MethylformamideHCID 31254—
Edukt2-Phenoxybenzoic acidHCID 75237—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
ProduktN-methyl-2-(2-phenoxyphenyl)-2-oxoacetamideHCID 1178009161%

Reaktionsbedingungen

Temperatur10 °C

Reaktionsschritte

N-Methylformamide (2.36 g, 40.0 mmol) and triethyl amine (8.08 g, 80.0 mmol) were dissolved in toluene (40 ml). Trichloromethylchloroformate (3.96 g, 20.0 mmol) was added dropwise slowly under ice-cooling while maintaining the inner temperature at 10° C. or lower. The mixture was stirred at the same temperature for 1 hour. A large amount of insoluble materials were precipitated. To the mixture was added 2-phenoxybenzoyl chloride which was prepared from 2-phenoxybenzoic acid (4.28 g, 20.0 mmol) and thionyl chloride (2.86 g, 24.0 mmol). The resulting mixture was stirred at bath temperature of 40° to 50° C. for 26 hours. 5N-Hydrochloric acid (12 ml) and acetone (20 ml) were added, and the mixture was stirred for 12 hours. Water was added to the mixture, which was then extracted with toluene and purified by column chromatography on silica gel to obtain the title compound (3.11 g, Yield: 61.0%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05414122
Quelldatensatzuspto-grants-1995_05
ORD IDord-3f1a560936404ceab29a4525d3e42212
Quellennotizuspto-grants-1995_05