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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43936생성일: 2026년 10월 24일

Water → HCID 68406269, 화합물

https://huagongshe.com/ko/reaction/43936

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물1-IodopropaneHCID 33643—
반응물Benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylateHCID 21981786—
용매TetrahydrofuranHCID 8028—
생성물HCID 68406269HCID 6840626926.7%

반응 단계

A solution of benzyl 4-[(tert-butoxycarbonyl)amino]piperidine-1-carboxylate obtained in Example (241a) (1.00 g, 2.99 mmol) in THF (5 mL) was added to a suspension of sodium hydride (55%) (261 mg, 5.98 mmol) in THF (25 mL) at 0° C. Subsequently, propyl iodide (1.46 mL, 15.0 mmol) was added at 0° C., and the mixture was stirred at room temperature for 22 hours. Thereafter, sodium hydride (55%) (130 mg, 2.99 mmol) and propyl iodide (0.58 mL, 5.98 mmol) were added, and the mixture was heated under reflux for 22 hours. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. Thereafter, the combined organic layers were washed with brine and dried over anhydrous magnesium sulfate. Following filtration, the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=5/1) to obtain 301 mg of the title compound as a pale yellow oily substance (27%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536197B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-62988030973a43508cfc013c231c063f
출처 메모uspto-grants-2013_09