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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726367Generated: October 30, 2026

HCID 57433448, compound → HCID 86599716, compound

https://huagongshe.com/reaction/1726367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57433448HCID 57433448—
ReactantHCID 58732860HCID 58732860—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductHCID 86599716HCID 86599716—

Reaction Steps

3-(5-Amino-3-fluoro-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester. Four cylinders charged with (S)-3-(3-fluoro-5-nitro-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester (50 g), 10% Pd(OH)2/C (5.0 g) and MeOH (300 mL) were subjected to hydrogenation under 50 psi H2. The mixture was stirred vigorously overnight. The mixture was filtered through a pad of diatomaceous earth and rinsed with methanol. The alcoholic solutions were combined and concentrated to give the aniline (S)-3-(5-amino-3-fluoro-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester as syrup in quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491826B2
Source datasetuspto-grants-2009_02
ORD IDord-3788d99c79be43a5bae749e7eadec915
Source noteuspto-grants-2009_02