Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 712949생성일: 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/712949
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-Benzyl-2-methylprop-2-en-1-amine | HCID 13788484 | — |
| 반응물 | tert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylate | HCID 22135564 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | Tert-butyl 4-[[benzyl(2-methylallyl)amino]methyl]-4-hydroxy-piperidine-1-carboxylate | HCID 68290967 | 100.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09181273B2 |
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| 출처 데이터셋 | uspto-grants-2015_11 |
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| ORD ID | ord-44db2e59244242a280a15098c40980be |
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| 출처 메모 | uspto-grants-2015_11 |
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