돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1469228생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1469228

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 번호US09006264B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-f5294d322e3a41acb139a391b41bed2f
출처 메모uspto-grants-2015_04