HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419462Generated: October 30, 2026
1-Methyl-4-{2-[3-(methyloxy)-4-nitrophenyl]ethyl}piperazine → 2-Methoxy-4-[2-(4-methylpiperazin-1-yl)ethyl]aniline
https://huagongshe.com/reaction/419462
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methyl-4-{2-[3-(methyloxy)-4-nitrophenyl]ethyl}piperazine | HCID 59452668 | — |
| Solvent | Ethylacetate methanol | HCID 21584119 | — |
| Product | 2-Methoxy-4-[2-(4-methylpiperazin-1-yl)ethyl]aniline | HCID 57416163 | 86% |
Reaction Steps
1-Methyl-4-{2-[3-(methyloxy)-4-nitrophenyl]ethyl}piperazine (0.6 g, 2.15 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 (0.42 g, 0.107 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 H2. The solution was filtered through celite and evaporated to afford the title compound of step D (0.460 g, 1.84 mmol, 86%). 1H NMR (400 MHz, CDCl3) δ ppm 6.60-6.64 (m, 3H), 3.82 (s, 3H), 3.64 (bs, 2H), 2.64-2.73 (m, 2H), 2.38-2.63 (m, 10H), 2.29 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093239B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-b5b519374f5245b2b8384b78c3629d47 |
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| Source note | uspto-grants-2012_01 |
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