تفاعل #155318
ord-16b0765578604f18b887cc78dc92088b
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1استخلاصfollowed by extraction
- 2غسيلThe extract was sequentially washed with an aqueous saturated sodium hydrogen solution
- 3تجفيفThe organic layer was dried over magnesium sulfate
- 4تركيزconcentrated to dryness under reduced pressure
- 5أخرىThe residue was purified
- 6تركيزThe purified product was concentrated to dryness under reduced pressure
الإجراء التجريبي
Benzhydrylidene(5-methylbenzofuran-7-yl)amine (17.9 g, 0.57 mmol) was dissolved in THF (150 ml). 5N Hydrochloric acid (50 ml) was added thereto, followed by stirring at room temperature for 2 hours. A 5N aqueous sodium hydroxide solution (40 ml) was added to the reaction mixture, followed by extraction using ethyl acetate. The extract was sequentially washed with an aqueous saturated sodium hydrogen solution and an aqueous saturated sodium chloride solution. The organic layer was dried over magnesium sulfate and concentrated to dryness under reduced pressure. The residue was purified using silica gel column chromatography (n-hexane:ethyl acetate=50:1→10:1). The purified product was concentrated to dryness under reduced pressure, giving a dark brown oily substance of 5-methylbenzofuran-7-ylamine (2.5 g, yield: 30%).