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HRID 482565생성일: 2026년 10월 25일

Benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate → 4-(N-Boc-amino)piperidine

https://huagongshe.com/reaction/482565

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylateHCID 21981786—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물4-(N-Boc-amino)piperidineHCID 723833100%

반응 단계

N-CBZ-4-(BOC-amino)-piperidine (3.0 g, 9.0 mmol) was dissolved in ethanol (100 mL) and transferred into a Parr shaker bottle. After adding 10% palladium on carbon (0.5 g), the mixture was shaken under an atmosphere of hydrogen at 50 psi for 0.75 h on a Parr apparatus. The catalyst was removed by filtration through a pad of Celite. The filter cake was washed with ethanol and the combined filtrate and washings were concentrated in vacuo to yield 1.8 g (100%) of crude 4-(BOC-amino)-piperidine as a pale yellow oil. This product was used immediately in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05798337
출처 데이터셋uspto-grants-1998_08
ORD IDord-e44a2a2a49a9468baf915e63b5283c87
출처 메모uspto-grants-1998_08