Reacción #77808
ord-166dbfddd38c4b35b4a216d8319fea93
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Temperaturaunder cooling with ice
- 2workup.STIRRINGwas stirred further for 2 hours at 30° C
- 3workup.DISTILLATIONSolvent was distilled off under reduced pressure, and 25% aqueous ammonia
- 4workup.ADDITIONwas added to the residue, which
- 5Extracciónwas extracted with ethyl acetate
- 6LavadoThe organic layer was washed with water and saturated brine in sequence
- 7Secadodried over anhydrous sodium sulfate
- 8workup.DISTILLATIONSolvent was distilled off under reduced pressure
- 9Otrothe residue obtained
- 10Otrowas crystallized from hexane
- 11Filtraciónethyl acetate=1:1, and then the crystals were collected by filtration
Procedimiento
To a solution of 2.26 g of 5-amino-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide in 27 ml of acetone and 11 ml of methanol were added 5.6 ml of 47% solution of hydrobromic acid, 540 mg of sodium nitrite and 2 ml of water under cooling with ice, and the mixture was stirred for 10 minutes. To the reaction mixture were added 3.00 g of acrylamide, and, after heated to 30° C., 135 mg of cupric oxide were added little by little, and the mixture was stirred further for 2 hours at 30° C. Solvent was distilled off under reduced pressure, and 25% aqueous ammonia was added to the residue, which was extracted with ethyl acetate. The organic layer was washed with water and saturated brine in sequence and dried over anhydrous sodium sulfate. Solvent was distilled off under reduced pressure, the residue obtained was crystallized from hexane:ethyl acetate=1:1, and then the crystals were collected by filtration to obtain 1.55 g of 5-(2-bromo-2-carbamoylethyl)-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide as colorless crystals.