反应详情

To a dry 1-L three-necked round-bottom flask equipped with a nitrogen inlet and overhead stirrer was charged 3-(3-quinolyl)-2-propyn-1-ol (15.81 g, 86.39 mmol), di-tert-butyl dicarbonate (22.48 g, 103 mmol, 1.19 equiv), n-tetrabutyl ammonium hydrogen sulfate (0.86 g, 2.54 mmol, 0.029 equiv) and methylene chloride (300 mL). The resulting suspension was mechanically stirred while a 25% w/w aqueous NaOH solution (38 g) was added in over a period of 5 minutes. The biphasic mixture which resulted was stirred for 4 hours after which time the reaction was found to be complete by HPLC and TLC. The mixture was diluted with water (200 mL) and methylene chloride (100 mL). After stirring for 10 minutes and settling for 15 minutes the layers were separated. The organic layer was washed with water (1×200 mL) and 20% aq., NaCl (1×200 mL). The organic was then stirred with 15 g of sodium sulfate, filtered and then stripped to an oil under reduced pressure. The residual oil was taken up in isopropyl acetate/ hexane (1:1, 100 mL) and passed through a small pad of silica gel (8 g). The pad was rinsed with the same eluent (100 mL). The combined filtrates were concentrated under reduced pressure and rigorously dried in a vacuum oven to yield the 3-(3-quinolyl)-2-propyn-1ol t-butyl carbonate as a light orange-yellow colored oil: 24.50 g, 100%.

1. additionwas added in over a period of 5 minutes
2. customThe biphasic mixture which resulted
3. stirringAfter stirring for 10 minutes
4. waitsettling for 15 minutes
5. customthe layers were separated
6. washThe organic layer was washed with water (1×200 mL) and 20% aq.
7. stirringThe organic was then stirred with 15 g of sodium sulfate
8. filtrationfiltered
9. washThe pad was rinsed with the same eluent (100 mL)
10. concentrationThe combined filtrates were concentrated under reduced pressure
11. customrigorously dried in a vacuum oven