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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253060생성일: 2026년 10월 26일

Water → Benzyl 4-methoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/253060

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물Benzyl 4-Hydroxy-1-piperidinecarboxylateHCID 2794620—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물Benzyl 4-methoxypiperidine-1-carboxylateHCID 2302430145%

반응 단계

To a solution of 1-benzyloxycarbonyl-4-hydroxypiperidine (1.3 g) in dimethylformamide (10 mL) was added sodium hydride (360 mL) under ice cooling and the mixture was stirred at room temperature under nitrogen-gas atmosphere for 1 hours. To the reaction mixture was added methyl iodide (374 μL) under ice-cooling and the mixture was stirred at the same temperature for 1 hour and at room temperature for 2 hours. To the reaction mixture was added water and ethyl acetate and the mixture was stirred. The organic layer washed with a brine, dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo and the resultant crude product was purified by column chromatography on silica gel (solvent: hexane/ethyl acetate=88/12 to 70/30) to obtain 1-benzyloxycarbonyl-4-methoxypiperidine (622 mg, yield: 45%) as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872006B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-e9dd1c0189ef49e99991622f5a437a99
출처 메모uspto-grants-2011_01