Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Benzylpiperidine → 4-Benzyl-1-(3-hydroxy-1-methylpropyl)piperidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Benzylpiperidine | HCID 31738 | — |
| 반응물 | Ethyl trans-crotonate | HCID 429065 | — |
| 반응물 | Ethyl 3-(4-benzylpiperidin-1-yl)butyrate | HCID 18621512 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | 4-Benzyl-1-(3-hydroxy-1-methylpropyl)piperidine | HCID 12972965 | 74% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06218404B1 |
| 출처 데이터셋 | uspto-grants-2001_04 |
| ORD ID | ord-28e8e8180f714be6b0b0588971ac9074 |
| 출처 메모 | uspto-grants-2001_04 |