Reaktion #2517

Reaktionsgleichung

sodium bicarbonate

o-anisidine

4-nitrobenzoic acid

1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride

→

title compound

Ausbeute 87.5%

4-Nitro-N-(2-methoxyphenyl)benzamide

Ausbeute 87.5%

Lösungsmittel

methylene chloride

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturWith cooling in an ice bath
2. 2
   Extraktionextracted with methylene chloride
3. 3
   Waschenwashed with water and saturated brine in that order
4. 4
   TrocknenAfter drying on anhydrous magnesium sulfate
5. 5
   Sonstigethe solvent was removed by evaporation
6. 6
   Sonstigethe resulting solid material was purified by silica gel column chromatography (methylene chloride)

Vorschrift

With cooling in an ice bath, 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC.HCl) (630 mg, 3.29 mmol) was added to 15 ml of methylene chloride solution containing o-anisidine (368 mg, 2.99 mmol) and 4-nitrobenzoic acid (500 mg, 2.99 mmol). After 1 hour of stirring at the same temperature, the reaction mixture was roughly adjusted to pH 8 with saturated sodium bicarbonate aqueous solution, extracted with methylene chloride and then washed with water and saturated brine in that order. After drying on anhydrous magnesium sulfate, the solvent was removed by evaporation, and the resulting solid material was purified by silica gel column chromatography (methylene chloride) to obtain 712 mg (87.4%) of the title compound in the form of yellow powder.

Quelle