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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419457Generated: October 25, 2026

4-{2-[2-Fluoro-5-(methyloxy)-4-nitrophenyl]ethyl}morpholine → 5-Fluoro-2-(methyloxy)-4-[2-(4-morpholinyl)ethyl]aniline

https://huagongshe.com/reaction/419457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-{2-[2-Fluoro-5-(methyloxy)-4-nitrophenyl]ethyl}morpholineHCID 59452916—
SolventEthyl AcetateHCID 8857—
Product5-Fluoro-2-(methyloxy)-4-[2-(4-morpholinyl)ethyl]anilineHCID 5945288656.2%

Reaction Steps

4-{2-[2-fluoro-5-(methyloxy)-4-nitrophenyl]ethyl}morpholine (0.4 g, 1.4 mmol) was placed in a 100 mL high pressure vessel and dissolved in 30 mL of EtOAc. 5 wt % Platinum(sulfided)/carbon (0.274 g, 0.07 mmol) was added followed quickly by a rubber septum. The flask was evacuated and filled with N2 six times to remove any 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 any hydrogen. The solution was filtered through celite and evaporated to give the title compound of step B (0.2 g, 0.79, 56%). 1H NMR (400 MHz, DMSO-d6) δ ppm 6.69 (d, J=6.97 Hz, 1H), 6.40 (d, J=11.36 Hz, 1H), 4.97 (bs, 2H), 3.86-3.98 (m, 2H), 3.78-3.86 (m, 2H), 3.72 (s, 3H), 3.38-3.49 (m, 2H), 3.10-3.21 (m, 2H), 2.99-3.10 (m, 2H), 2.86-2.97 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-f407752c85954ea5b4fb1ac4027c4989
Source noteuspto-grants-2012_01