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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-(3-fluorobenzylidene)piperidine-1-carboxylateHCID 70984044—
CatalystPalladium hydroxideHCID 9942167—
SolventAcetic AcidHCID 176—
Product4-[(3-Fluorophenyl)methyl]piperidineHCID 1072814185.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290472B2
Source datasetuspto-grants-2016_03
ORD IDord-36ee5cd19577485f80c6360881a56c36
Source noteuspto-grants-2016_03