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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121750Generated: November 2, 2026

3-(4-Nitrophenyl)pyridine → 4-(Pyridin-3-yl)aniline

https://huagongshe.com/reaction/2121750

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Nitrophenyl)pyridineHCID 231504—
CatalystPalladiumHCID 23938—
SolventDichloromethaneHCID 6344—
Product4-(Pyridin-3-yl)anilineHCID 45952295%

Reaction Steps

In a flame-dried r.b. flask equipped with a magnetic stirring bar was dissolved 3-(4-nitrophenyl)pyridine (131 mg, 0.655 mmol) and 10% Pd on C (10 mg) in anhydrous CH2Cl2 (3mL) was added. The flask was repeatedly evacuated and filled with N2 to remove any residual O2, and then H2 gas was introduced. The solution was stirred at rt for 18 h, filtered though a Celite™ plug and concentrated in vacuo to give the desired amine (105 mg, 95%) as an off-white solid. Data for 3-(4-aminophenyl)pyridine: Rf=0.17 (silica gel, methanol/CHCl3, 5/95); 1H NMR (400 MHz, acetone-d6) 8.77 (d, J=2.3, 1H), 8.42 (dd, J=6.4, 1.6, 1H), 7.88 (m, 1H), 7.4 (d, J=8.5, 2H), 7.33 (m, 1H), 6.78 (d, J=8.5, 2H), 4.86 (br s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696459B1
Source datasetuspto-grants-2004_02
ORD IDord-5d8f23664c984d5b933cf71eb5f3bc96
Source noteuspto-grants-2004_02