반응 #52175
ord-688a5ddf0e974ed988f40d5885b8b18c
반응 방정식
반응 조건
후처리
- 1온도under cooling with ice
- 2기타to terminate
- 3기타the reaction
- 4추출After the extraction with ethyl acetate (10 ml×3)
- 5기타dried
- 6농축concentrated under reduced pressure
- 7기타The residue was purified by the silica gel column chromatography (hexane, hexane/ethyl acetate, 100/1)
- 8기타to obtain an intermediate product
- 9workup.STIRRINGThe reaction mixture was stirred at room temperature for 4 days
- 10workup.STIRRINGAfter stirring at room temperature for 9 days
- 11추출The resultant mixture was extracted with water (10 ml)
- 12추출After the extraction with DCM (10 ml×3)
- 13기타dried
- 14농축concentrated under reduced pressure to quantitatively obtain 481 mg of the intended compound
실험 절차
Methyl phenylsulfonylacetate (0.64 ml, 4.0 mmol) was diluted with DMF (5 ml). Sodium hydride (384 mg, 16 mmol) and ethyl bromide (1.19 ml, 16 mmol) were added thereto under argon atmosphere. The mixture was stirred at room temperature overnight. Water was added to the reaction mixture under cooling with ice to terminate the reaction. After the extraction with ethyl acetate (10 ml×3), the organic layers were combined together, dried and concentrated under reduced pressure. The residue was purified by the silica gel column chromatography (hexane, hexane/ethyl acetate, 100/1) to obtain an intermediate product. The intermediate product (532 mg, 1.97 mmol) was dissolved in THF (4 ml). Water (70.9 μl, 3.84 mmol) and tBuOK (1.77 g, 15.8 mmol) were added to the obtained solution. The reaction mixture was stirred at room temperature for 4 days. Additional water (35.5 μl, 1.97 mmol) and tBuOK (1.55 g, 13.8 mmol) were added to the obtained solution. After stirring at room temperature for 9 days, the reaction mixture was diluted with DCM (10 ml). The resultant mixture was extracted with water (10 ml). pH of the aqueous layer was adjusted to 2. After the extraction with DCM (10 ml×3), the organic layers were combined together, dried and concentrated under reduced pressure to quantitatively obtain 481 mg of the intended compound.