HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131049Erstellt: 24. Oktober 2026
Potassium Hydroxide → 3-Butyl-1-(4-methoxy-benzyl)-piperidine
https://huagongshe.com/de/reaction/131049
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 1-[1-(4-Methoxy-benzyl)-piperidin-3-yl]-butan-1-one | HCID 59730198 | — |
| Lösungsmittel | Diethylene Glycol | HCID 8117 | — |
| Produkt | 3-Butyl-1-(4-methoxy-benzyl)-piperidine | HCID 59730401 | 89% |
Reaktionsschritte
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).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07381719B2 |
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| Quelldatensatz | uspto-grants-2008_06 |
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| ORD ID | ord-6e0803076ca548148366ebe5a232277d |
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| Quellennotiz | uspto-grants-2008_06 |
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