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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419451Generated: October 29, 2026

1-{2-[2-Fluoro-5-(methyloxy)-4-nitrophenyl]ethyl}piperidine → 5-Fluoro-2-(methyloxy)-4-[2-(1-piperidinyl)ethyl]aniline

https://huagongshe.com/reaction/419451

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-{2-[2-Fluoro-5-(methyloxy)-4-nitrophenyl]ethyl}piperidineHCID 59452971—
SolventEthyl AcetateHCID 8857—
Product5-Fluoro-2-(methyloxy)-4-[2-(1-piperidinyl)ethyl]anilineHCID 5945293081%

Reaction Steps

1-{2-[2-fluoro-5-(methyloxy)-4-nitrophenyl]ethyl}piperidine (0.81 g, 2.87 mmol) was placed in a 100 mL high pressure vessel and dissolved in 30 mL of EtOAc. 5 wt % Platinum(sulfided)/carbon (0.559 g, 0.143 mmol) was added followed quickly by a rubber septum. The flask was evacuated and filled with N2 six times to remove oxygen. The vessel was then pressurized with H2 (50 psi). The solution stirred overnight. The next morning the vessel was evacuated and filled with N2 six times to remove H2. The solution was filtered through celite and evaporated to afford the title compound of step D (0.586 g, 2.32 mmol, 81%). 1H NMR (400 MHz, CD3OD) δ ppm 6.72 (d, J=6.96 Hz, 1H), 6.46 (d, J=11.35 Hz, 1H), 3.81 (s, 3H), 3.21-3.27 (m, 2H), 3.13-3.21 (m, 4H), 2.93-2.99 (m, 2H), 1.82-1.89 (m, 4H), 1.62-1.71 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-ddc04fcc29cb49c7afb545f617ea63f5
Source noteuspto-grants-2012_01