HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228500Generated: October 25, 2026
Potassium Hydroxide → 3-Butyl-1-(4-methoxy-benzyl)-piperidine
https://huagongshe.com/reaction/228500
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-[1-(4-Methoxy-benzyl)-piperidin-3-yl]-butan-1-one | HCID 59730198 | — |
| Solvent | Diethylene Glycol | HCID 8117 | — |
| Product | 3-Butyl-1-(4-methoxy-benzyl)-piperidine | HCID 59730401 | 89% |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560463B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-777cd9e8c37d4ae192acd6077e7596a1 |
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| Source note | uspto-grants-2009_07 |
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