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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419497Generated: October 30, 2026

1-Methyl-4-{2-[3-(ethyloxy)-4-nitrophenyl]ethyl}piperazine → 2-(Ethyloxy)-4-[2-(4-methyl-1-piperazinyl)ethyl]aniline

https://huagongshe.com/reaction/419497

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-4-{2-[3-(ethyloxy)-4-nitrophenyl]ethyl}piperazineHCID 59452783—
SolventEthylacetate methanolHCID 21584119—
Product2-(Ethyloxy)-4-[2-(4-methyl-1-piperazinyl)ethyl]anilineHCID 59452821101.8%

Reaction Steps

1-methyl-4-{2-[3-(ethyloxy)-4-nitrophenyl]ethyl}piperazine (0.373 g, 1.14 mmol) was placed in a 100 mL high pressure vessel and dissolved in 30 mL of 1 to 1 EtOAc/MeOH. 5 wt % Platinum(sulfided)/carbon (0.223 g, 0.057 mmol) was added followed quickly by a screw cap septum. The flask was evacuated and filled with N2 six times to remove any oxygen. The vessel was then pressurized with H2 (balloon). The solution stirred overnight. The next morning the vessel was evacuated and filled with N2 six times to remove any H2. The solution was filtered through celite and evaporated to afford the title compound of step D (0.308 g, 1.16 mmol, 100%). 1H NMR (400 MHz, CDCl3) δ ppm 6.57-6.65 (m, 3H), 3.99-4.08 (m, 2H), 3.62-3.74 (m, 2H), 2.65-2.75 (m, 2H), 2.47-2.59 (m, 8H), 2.31 (s, 3H), 1.36-1.45 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-fc06f982371b47c6beeadb9e05dc61bf
Source noteuspto-grants-2012_01