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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72869생성일: 2026년 10월 25일

N-Benzyl-2-methylprop-2-en-1-amine → Tert-butyl 4-[[benzyl(2-methylallyl)amino]methyl]-4-hydroxy-piperidine-1-carboxylate

https://huagongshe.com/reaction/72869

반응식

참여 물질

역할이름HCID투입량
반응물N-Benzyl-2-methylprop-2-en-1-amineHCID 13788484—
반응물tert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylateHCID 22135564—
용매EthanolHCID 702—
생성물Tert-butyl 4-[[benzyl(2-methylallyl)amino]methyl]-4-hydroxy-piperidine-1-carboxylateHCID 68290967100.1%

반응 조건

온도80 °C

반응 단계

A mixture of N-benzyl-2-methyl-prop-2-en-1-amine (0.57 g, 3.52 mmol) and tert-butyl 1-oxa-6-azaspiro[2.5]octane-6-carboxylate (0.75 g, 3.52 mmol) in ethanol (4 mL) was heated at 80° C. in a sealed vial for 16 hours. The reaction mixture was cooled and concentrated in vacuo to give tert-butyl 4-[[benzyl(2-methylallyl)amino]methyl]-4-hydroxy-piperidine-1-carboxylate (1.32 g, 100%) as a colorless oil. ESI-MS m/z calc. 374.5. Found 375.7 (M+1)+; Retention time: 1.24 minutes (3 min run).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828996B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-cf83464a72944814bed200a05ceac889
출처 메모uspto-grants-2014_09