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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1363522생성일: 2026년 10월 23일

Ethyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylate → Ethyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/ko/reaction/1363522

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylateHCID 22708806—
촉매Palladium hydroxideHCID 9942167—
용매EthanolHCID 702—
생성물Ethyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylateHCID 14049029—

반응 단계

A mixture of ethyl 4-hydroxy-4-(nitromethyl)piperidine-1-carboxylate (5.2 g, 22.4 mmol) and 20% palladium hydroxide on carbon (0.50 g) in ethanol (190 mL) was hydrogenated at 35 psi (2.4×105 Pa) on a Parr apparatus for 5 h. The mixture was filtered through CELITE filter agent and the filtrate was concentrated. By 1H NMR analysis, the reaction was incomplete and the crude material was subjected to the reaction conditions again with fresh 20% palladium hydroxide on carbon (0.50 g) for another 24 h. The mixture was filtered through CELITE filter agent and the filtrate was concentrated to provide ethyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate, which was concentrated from chloroform to remove residual ethanol before using in the next reaction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07884207B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-1387acf13928454e99b12c92bfa81453
출처 메모uspto-grants-2011_02