تفاعل #77812
ord-faaa6191dbe04481811664c513cd2e9a
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1workup.STIRRINGwas stirred further for 1 hour at 40 to 50° C
- 2workup.DISTILLATIONSolvent was distilled off under reduced pressure, and 25% aqueous ammonia
- 3workup.ADDITIONwas added to the residue, which
- 4استخلاصwas extracted with ethyl acetate
- 5غسيلThe organic layer was washed with water and saturated brine in sequence
- 6تجفيفdried over anhydrous sodium sulfate
- 7workup.DISTILLATIONSolvent was distilled off under reduced pressure
- 8أخرىthe residue obtained
- 9أخرىwas crystallized from hexane-ethyl acetate
- 10ترشيحthe crystals were collected by filtration
الإجراء التجريبي
To a solution of 17.3 g of 5-amino-2-methoxy-N-(4-trifluoromethylbenzyl)benzamide in 170 ml of acetone and 85 ml of methanol were added 43 ml of 47% solution of hydrobromic acid and 17 ml of aqueous solution of 4.15 g of sodium nitrite under cooling with ice-salt, and the mixture was stirred for 10 minutes. To the reaction mixture were added 26 ml of methyl acrylate, and, after heated to 30° C., 1.04 g of cupric oxide were added little by little, and the mixture was stirred further for 1 hour at 40 to 50° 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, and the residue obtained was crystallized from hexane-ethyl acetate, then the crystals were collected by filtration to obtain 10.3 g of methyl 2-bromo-3-[4-methoxy-3-[N-(4-trifluoromethylbenzyl)]carbamoylphenyl]-propionate as light brown crystals.