HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928047Generated: October 30, 2026
Benzyl 4-(3-fluorobenzylidene)piperidine-1-carboxylate → 4-[(3-Fluorophenyl)methyl]piperidine
https://huagongshe.com/reaction/928047
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl 4-(3-fluorobenzylidene)piperidine-1-carboxylate | HCID 70984044 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-[(3-Fluorophenyl)methyl]piperidine | HCID 10728141 | 85.3% |
Reaction Steps
A mixture of benzyl 4-(3-fluorobenzylidene)piperidine-1-carboxylate (Intermediate 181, 1.05 g), 20% palladium hydroxide on carbon (0.227 g), IMS (30 mL) and acetic acid (10 mL) was degassed by nitrogen/vacuum purging. The mixture was placed under an atmosphere of hydrogen with rapid stirring. After 2 hours the mixture was filtered and the filtrate was diluted with water (40 mL) and neutralized with Na2CO3. The solution was saturated with sodium chloride, extracted with ethyl acetate dried (MgSO4) and filtered. The filtrate was concentrated in vacuo and the residue was dissolved in a mixture of methanol and water (20 mL, 1:1) and passed down a SCX-2 column. The product was eluted with 2M ammonia to give 4-(3-fluorobenzyl)piperidine (0.532 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290472B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-36ee5cd19577485f80c6360881a56c36 |
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| Source note | uspto-grants-2016_03 |
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