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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014220Generated: November 2, 2026

HCID 59442053, compound → HCID 59441839, compound

https://huagongshe.com/reaction/1014220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59442053HCID 59442053—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 59441839HCID 5944183980%

Reaction Steps

A solution of 1-(1-methylethyl)-4-[4-(methyloxy)-3-nitrophenyl]piperazine (0.6 g, 2.15 mmol) in absolute ethanol (100 mL) was hydrogenated with 10% Pd/C (Lancaster) at 50 psi overnight. The catalyst was removed by vacuum filtration through a celite pad, rinsed with methanol, the filtrate was concentrated under reduced pressure, and the crude aniline was purified by chromatography on SiO2 (dichloromethane to 10% methanol/dichloromethane with 0.1% NH4OH) to provide 5-[4-(1-methylethyl)-1-piperazinyl]-2-(methyloxy)aniline as a white solid (0.42 g, 80%). ESIMS (M+H)+=250.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-ccd1f54ebca74263a8b0528cb6e8dd46
Source noteuspto-grants-2011_07