تفاعل #1179947
ord-3532f5372dd1411a8e850f2894a88670
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.ADDITIONwas added to the solution
- 2درجة الحرارةAfter the reaction mixture was cooled
- 3أخرىthe organic layer was separated
- 4غسيلThe organic layer was washed with water
- 5تجفيفa saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate
- 6workup.DISTILLATIONdistilled under reduced pressure
- 7أخرىto remove the solvent
- 8أخرىThe residue was purified by a column chromatography (eluent; chloroform:methanol=7:1)
الإجراء التجريبي
In 8 mL of N,N-dimethylformamide was dissolved 0.80 g of 5-[2-(3-chloropropoxy)ethyl]-1-benzothiophene, and 1.20 g of N-(3-azetidinyl)acetamide was added to the solution, after which the resulting mixture was stirred at 90° C. for 12 hours. After the reaction mixture was cooled, water and ethyl acetate were added thereto and the organic layer was separated. The organic layer was washed with water and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. The residue was purified by a column chromatography (eluent; chloroform:methanol=7:1) to obtain 0.39 g of N-(1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinyl)acetamide as a light-yellow oil.