반응 #167498
ord-aacd1bf222fa4cfc82ebf5fc2d04c7e8
반응 방정식
반응 조건
후처리
- 1온도while cooling with ice
- 2기타was returned to room temperature
- 3workup.DISTILLATIONthe solvent was distilled off under reduced pressure
- 4기타to thereby obtain a residue
- 5온도The mixture was refluxed for 45 minutes
- 6workup.DISTILLATIONThe solvent was distilled off under reduced pressure
- 7workup.ADDITIONa saturated aqueous solution of sodium hydrogen carbonate (Wako Pure Chemical Industries, Ltd.) was added to the concentrated residue, and mixture
- 8추출was extracted with ethyl acetate (Wako Pure Chemical Industries, Ltd.)
- 9세척The organic layer was washed with water and brine
- 10건조After that, the organic layer was dried with anhydrous sodium sulfate (Wako Pure Chemical Industries, Ltd.)
- 11workup.DISTILLATIONthe solvent was distilled off under reduced pressure
실험 절차
Compound 23 described above (0.17 g, 0.589 mmol) was dissolved in chloroform (4 mL) (Wako Pure Chemical Industries, Ltd.), and thionyl chloride (0.5 mL) (Wako Pure Chemical Industries, Ltd.) was added dropwise while cooling with ice. The mixture was returned to room temperature and stirred for 1 hour, and then the solvent was distilled off under reduced pressure, to thereby obtain a residue. The residue was dissolved in acetonitrile (4 mL) (Wako Pure Chemical Industries, Ltd.), and piperidine (0.19 g, 2.23 mmol) (Wako Pure Chemical Industries, Ltd.) was added thereto. The mixture was refluxed for 45 minutes and allowed to cool to room temperature. The solvent was distilled off under reduced pressure, and then a saturated aqueous solution of sodium hydrogen carbonate (Wako Pure Chemical Industries, Ltd.) was added to the concentrated residue, and mixture was extracted with ethyl acetate (Wako Pure Chemical Industries, Ltd.). The organic layer was washed with water and brine. After that, the organic layer was dried with anhydrous sodium sulfate (Wako Pure Chemical Industries, Ltd.), and the solvent was distilled off under reduced pressure. The residue was subjected to alumina column chromatography (n-hexane (Wako Pure Chemical Industries, Ltd.) as an eluent), to thereby obtain the title compound (0.17 g, 81% yield).