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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1861776생성일: 2026년 10월 26일

Ethyl 3-(4-benzylpiperidin-1-yl)butyrate → 4-Benzyl-1-(3-hydroxy-1-methylpropyl)piperidine

https://huagongshe.com/reaction/1861776

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참여 물질

역할이름HCID투입량
반응물Ethyl 3-(4-benzylpiperidin-1-yl)butyrateHCID 18621512—
반응물Aluminium lithium hydrideHCID 21226445—
용매TetrahydrofuranHCID 8028—
생성물4-Benzyl-1-(3-hydroxy-1-methylpropyl)piperidineHCID 1297296580%

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온도25 °C

반응 단계

To a solution of ethyl 3-(4-benzylpiperidin-1-yl)butyrate (0.60 g, 2.0 mmol) in dry THF (10 mL) was added portionwise LiAlH4 (0.15 g, 3.9 mmol). The resulting heterogeneous mixture was stirred at 25° C. for 2 h then quenched with MeOH. The resulting mixture was diluted with EtOAc (100 mL), washed with NH4Cl (100 mL) and brine (100 mL), dried and was concentrated under reduced pressure. The crude compound was purified by filtration on silica gel using CH2Cl2/MeOH as solvent to afford the title compound as a colorless solid (0.38 g, 80%): mp 74-76° C.; 1H NMR (CDCl3) δ1.00 (d, J=6.6 Hz, 3H), 1.15-1.45 (m, 3H), 1.50-1.65 (m, 1H), 1.65-1.80 (m, 2H), 1.85-2.15 (m, 3H), 2.40-2.60 (m, 3H), 2.82 (bd, J=11.1 Hz, 1H), 2.90-3.10 (m, 2H), 3.80-4.00 (m, 2H), 6.55 (bs, 1H), 7.19 (t, J=7.2 Hz, 2H), 7.24 (d, J=6.9 Hz, 1H), 7.32 (t, J=7.2 Hz, 2H); MS (m/z) 247, 248, 232, 202, 91. Anal. Calcd for C16H25NO: C, 77.68, H 10.18; N, 5.66. Found C, 77.56; H 10.22; N, 5.63.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06534522B2
출처 데이터셋uspto-grants-2003_03
ORD IDord-d041f354dfe94a9dacf2055371649c04
출처 메모uspto-grants-2003_03