Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44689생성일: 2026년 10월 23일
Ethyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylate → Ethyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate
https://huagongshe.com/ko/reaction/44689
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylate | HCID 22708806 | — |
| 촉매 | Palladium hydroxide | HCID 9942167 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | Ethyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08541438B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-e97a7697d026407fb91118f4daf04744 |
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| 출처 메모 | uspto-grants-2013_09 |
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