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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495446Generated: October 29, 2026

tert-Butyl 4-(3-fluoro-4-methoxybenzylidene)piperidine-1-carboxylate → HCID 69354983, compound

https://huagongshe.com/reaction/495446

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(3-fluoro-4-methoxybenzylidene)piperidine-1-carboxylateHCID 69356823—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 69354983HCID 6935498399%

Reaction Steps

A solution of 4-(3-fluoro-4-methoxy-benzylidene)-piperidine-1-carboxylic acid tert-butyl ester (4.7 g, 14.6 mmol) in methanol (400 mL) was allowed to stir under atmospheric pressure of hydrogen at room temperature in the presence of 10% palladium on carbon (0.8 g) for 16 hours. Removal of the catalyst by filtration and evaporation of the filtrate gave a crude oil. Silica gel chromatography eluting with ethyl acetate in hexane (10%) gave the title compound (4.3 g, 99%) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939871B2
Source datasetuspto-grants-2005_09
ORD IDord-e9bc15d1ce524b47b1cd62614dc5ee10
Source noteuspto-grants-2005_09