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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 579781생성일: 2026년 10월 26일

Methanol → Ethyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/579781

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Ethyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylateHCID 22708806—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매Acetic AcidHCID 176—
생성물Ethyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylateHCID 14049029—

반응 단계

A mixture of 73 parts of ethyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylate, 400 parts of methanol and 150 parts of acetic acid was hydrogenated in the Parr-apparatus with 5 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. To the residue was added crushed ice and the whole was alkalized with potassium hydroxide. The aqueous phase was salted out with potassium carbonate and the product was extracted with benzene. The extract was dried, filtered and evaporated, yielding 63.5 parts of ethyl 4-(aminomethyl)-4-hydroxy-1-piperidinecarboxylate; mp. ±82° C. (intermediate 6).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04749702
출처 데이터셋uspto-grants-1988_06
ORD IDord-57e94454633f4bb884ce95040a1c1a8f
출처 메모uspto-grants-1988_06