反应详情

温度

60 °C

A commercially available reagent of ethyl (S)-2-tert-butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionate (4.84 g, 15.6 mmol) was dissolved in N,N-dimethylformamide (39 mL), and 1-bromo-2-butyne (1.65 mL, 18.8 mmol) and potassium carbonate (3.25 g, 23.5 mmol) were then added at room temperature. After stirring at 60° C. for 6 hours, and the reaction solution was cooled to room temperature. 1-Bromo-2-butyne (0.55 mL, 6.28 mmol) was added at room temperature, and the mixture was then stirred at 60° C. for 5 hours. The reaction solution was cooled to room temperature, and potassium carbonate (0.433 g, 3.13 mmol) was then added. After stirring at 60° C. for 4.5 hours, the reaction solution was cooled to room temperature. Water (70 mL) was added, and the mixture was then extracted twice with ethyl acetate (70 mL). The organic layer was washed with saturated aqueous solution (30 mL) of sodium chloride, dried over anhydrous sodium sulfate, and filtered. The solvent was distilled off under reduced pressure. The residue was purified on Biotage (silica gel, n-hexane/ethyl acetate) to obtain 5.02 g (13.9 mmol, yield 89%) of ethyl (S)-2-tert-butoxycarbonylamino-3-(4-but-2-ynyloxy-phenyl)-propionate.

1. temperaturethe reaction solution was cooled to room temperature
2. stirringthe mixture was then stirred at 60° C. for 5 hours
3. temperatureThe reaction solution was cooled to room temperature
4. stirringAfter stirring at 60° C. for 4.5 hours
5. temperaturethe reaction solution was cooled to room temperature
6. extractionthe mixture was then extracted twice with ethyl acetate (70 mL)
7. washThe organic layer was washed with saturated aqueous solution (30 mL) of sodium chloride
8. dry with materialdried over anhydrous sodium sulfate
9. filtrationfiltered
10. distillationThe solvent was distilled off under reduced pressure
11. customThe residue was purified on Biotage (silica gel, n-hexane/ethyl acetate)