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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1505882생성일: 2026년 10월 27일

Piperidine → 3-Methoxy-4-piperidin-1-ylmethylphenol

https://huagongshe.com/reaction/1505882

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물4-Hydroxy-2-MethoxybenzaldehydeHCID 519541—
반응물Sodium triacetoxyborohydrideHCID 5049666—
촉매Titanium isopropoxideHCID 11026—
용매DichloromethaneHCID 6344—
생성물3-Methoxy-4-piperidin-1-ylmethylphenolHCID 5826673730.8%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09216980B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-027c4cee7b1c42b4847c50d71cc53345
출처 메모uspto-grants-2015_12