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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131049생성일: 2026년 10월 24일

Potassium Hydroxide → 3-Butyl-1-(4-methoxy-benzyl)-piperidine

https://huagongshe.com/ko/reaction/131049

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물Ammonium ChlorideHCID 25517—
반응물1-[1-(4-Methoxy-benzyl)-piperidin-3-yl]-butan-1-oneHCID 59730198—
용매Diethylene GlycolHCID 8117—
생성물3-Butyl-1-(4-methoxy-benzyl)-piperidineHCID 5973040189%

반응 조건

온도120 °C

반응 단계

Combine 1-[1-(4-Methoxy-benzyl)-piperidin-3-yl]-butan-1-one (356.0 mg, 0.95 mmol), Diethylene glycol (15 mL), KOH (479.0 mg, 8.54 mmol), and Hydrazine-monohydrate (1.8 mL) at room temperature under a Nitrogen atmosphere. Heat the reaction mixture to 120° C. for 2 hours and then 220° C. for 24 hours. Cool reaction to room temperature and then pour the reaction mixture over sat NH4Cl (aq). Extract with Ethyl acetate, wash with brine, and dry over Na2SO4. Concentrate under reduced pressure and flash chromatograph using 3% 1N NH3MeOH in CH2Cl2 to give 220.7 mg (89% yield) of the title compound: 1H NMR (500 MHz, CDCl3); 0.7-0.9 (3H, m), 1.1-1.4 (4H, m), 1.5-1.7 (4H, m), 1.7 (1H, d), 1.9 (1H, t), 2.8 (2H, t), 3.4 (2H, dd), 3.6-3.7 (3H, m), 3.8 (3H, s), 6.8 (2H, d), 7.2 (2H, d); MS m/z 262 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381719B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-6e0803076ca548148366ebe5a232277d
출처 메모uspto-grants-2008_06