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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365629Generated: October 27, 2026

4-(1-Methylpyrrol-2-ylmethyl)nitrobenzene → 4-(1-Methylpyrrol-2-yl-methyl)aniline

https://huagongshe.com/reaction/365629

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1-Methylpyrrol-2-ylmethyl)nitrobenzeneHCID 23285794—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product4-(1-Methylpyrrol-2-yl-methyl)anilineHCID 23285967100%

Reaction Steps

4-(1-Methylpyrrol-2-ylmethyl)nitrobenzene (500 mg, 2.31 mmol) [prepared as described in Example 21, Step (b)], was dissolved in ethyl acetate and subjected to hydrogenation over 5% Pd/C (50 mg) at ambient temperature and atmospheric pressure. After 3 h the mixture was filtered and the filtrate was concentrated to give 4-(1-methylpyrrol-2-yl-methyl)aniline (430 mg, 100%) as a yellow oil. ##STR63##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127402
Source datasetuspto-grants-2000_10
ORD IDord-7750102a0099436c9283fccd80d31ac0
Source noteuspto-grants-2000_10