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HRID 228500作成日:2026年10月26日

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

https://huagongshe.com/reaction/228500

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物Hydrazine hydrate (1:1)HCID 24654—
反応物Ammonium ChlorideHCID 25517—
反応物1-[1-(4-Methoxy-benzyl)-piperidin-3-yl]-butan-1-oneHCID 59730198—
溶媒Diethylene GlycolHCID 8117—
生成物3-Butyl-1-(4-methoxy-benzyl)-piperidineHCID 5973040189%

反応条件

温度120 °C

反応手順

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 NH3 MeOH 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560463B2
出典データセットuspto-grants-2009_07
ORD IDord-777cd9e8c37d4ae192acd6077e7596a1
出典メモuspto-grants-2009_07