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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240595Generated: October 25, 2026

Ammonium formate → (R)-tert-butyl 3-(2-amino-5-fluorophenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/240595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant(R)-tert-butyl 3-(5-fluoro-2-nitrophenoxy)piperidine-1-carboxylateHCID 67395513—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(R)-tert-butyl 3-(2-amino-5-fluorophenoxy)piperidine-1-carboxylateHCID 58413198—

Reaction Steps

Amoniumformiate (1.0 g) was added into a suspension of (R)-tert-butyl 3-(5-fluoro-2-nitrophenoxy)piperidine-1-carboxylate and palladium on charcoal (125.0 mg) in anhydrous MeOH (10.0 ml) at room temperature. The reaction was stirred at room temperature overnight when LCMS analysis indicated consumption of the starting material. The solution was filtered through celite and washed with MeOH. The filtrate was concentrated in vacuo. The residue was triturated with diethylether to remove the ammoniumformiate residues. The solution was filtered and concentrated in vacuo. The residue was purified by chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648068B2
Source datasetuspto-grants-2014_02
ORD IDord-250dd16659d04b508156aa1c00a196e2
Source noteuspto-grants-2014_02