반응 #155318
ord-16b0765578604f18b887cc78dc92088b
반응 방정식
용매
반응 조건
후처리
- 1추출followed by extraction
- 2세척The extract was sequentially washed with an aqueous saturated sodium hydrogen solution
- 3건조The organic layer was dried over magnesium sulfate
- 4농축concentrated to dryness under reduced pressure
- 5기타The residue was purified
- 6농축The purified product was concentrated to dryness under reduced pressure
실험 절차
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%).