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HRID 1370013생성일: 2026년 10월 25일

Sodium Hydroxide → 3-(3-Quinolyl)-2-propyn-1-ol t-butyl carbonate

https://huagongshe.com/reaction/1370013

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Di-tert-butyl dicarbonateHCID 90495—
반응물3-Quinolin-3-ylprop-2-yn-1-olHCID 650142—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물3-(3-Quinolyl)-2-propyn-1-ol t-butyl carbonateHCID 131723396—

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06579986B2
출처 데이터셋uspto-grants-2003_06
ORD IDord-56a7c96508924bae84d6c02891d6bc94
출처 메모uspto-grants-2003_06