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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324553생성일: 2026년 10월 25일

4-Benzylpiperidine → 4-Benzyl-1-(3-hydroxy-1-methylpropyl)piperidine

https://huagongshe.com/reaction/324553

반응식

참여 물질

역할이름HCID투입량
반응물4-BenzylpiperidineHCID 31738—
반응물Ethyl trans-crotonateHCID 429065—
반응물Ethyl 3-(4-benzylpiperidin-1-yl)butyrateHCID 18621512—
용매IsopropanolHCID 3776—
생성물4-Benzyl-1-(3-hydroxy-1-methylpropyl)piperidineHCID 1297296574%

반응 단계

Ethyl 3-(4-benzylpiperidin-1-yl)butyrate. A solution of 4-benzyl piperidine (0.50 mL, 2.8 mmol) and ethyl crotonate (0.46 mL, 3.4 mol) in isopropanol (10 mL) was refluxed for 24 h and was concentrated in vacuo. The crude compound was purified by filtration on silica gel using CH2Cl2/MeOH as solvent to afford the title compound as a pale yellow oil (0.64 g, 74%): 1H NMR (CDCl3) δ 1.09 (d, J=6.6 Hz, 3H), 1.30 (t, J=6.9 Hz, 3H), 1.20-1.40 (m, 2H), 1.45-1.61 (m, 1H), 1.68 (bd, J=12.3 Hz, 2H), 2.10-2.35 (m, 3H), 2.57 (d, J6.9 Hz, 2H), 2.50-2.70 (m, 1H), 2.82 (bd, J=10.8 Hz, 2H), 3.15-3.30 (m, 1H), 4.18 (q, J=6.9 Hz, 2H), 7.18 (d, J=7.2 Hz, 2H), 7.24 (m, 1H), 7.32 (t, J=6.9 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06218404B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-28e8e8180f714be6b0b0588971ac9074
출처 메모uspto-grants-2001_04