Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Piperidine → 3-Methoxy-4-piperidin-1-ylmethylphenol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | 4-Hydroxy-2-Methoxybenzaldehyde | HCID 519541 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 촉매 | Titanium isopropoxide | HCID 11026 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-Methoxy-4-piperidin-1-ylmethylphenol | HCID 58266737 | 30.8% |
반응 단계
To a pre-stirred solution of 4-hydroxy-2-methoxybenzaldehyde (1.02 g, 6.7 mmol), titanium isopropoxide (2.14 mL, 7.0 mmol) and piperidine (0.70 mL, 7.0 mmol) in DCM (20 mL) was added sodium triacetoxyborohydride (2.84 g, 13.4 mmol) in portions. After 3 h the reaction mixture was quenched by the addition of methanol (1.0 mL) and then the solvents were removed under reduced pressure to afford a residue. The resultant residue was then loaded onto an SCX-2 cartridge (10 g) and eluted with 2N ammonia in methanol to afford the title compound (456 mg, 30%). 1H NMR (CD3OD, 300 MHz): 7.17 (d, J=8.3 Hz, 1H), 6.51 (d, J=2.3 Hz, 1H), 6.43 (dd, J=8.2, 2.2 Hz, 1H), 4.07 (s, 2H), 3.84 (s, 3H), 3.16-2.99 (m, 4H), 1.84-1.73 (m, 4H), 1.67-1.56 (m, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09216980B2 |
| 출처 데이터셋 | uspto-grants-2015_12 |
| ORD ID | ord-027c4cee7b1c42b4847c50d71cc53345 |
| 출처 메모 | uspto-grants-2015_12 |