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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173806Generated: November 4, 2026

5-Nitro-2-(4-(trifluoromethyl)phenyl)pyridine → 6-(4-(Trifluoromethyl)phenyl)pyridin-3-amine

https://huagongshe.com/reaction/2173806

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Nitro-2-(4-(trifluoromethyl)phenyl)pyridineHCID 67980851—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product6-(4-(Trifluoromethyl)phenyl)pyridin-3-amineHCID 5964137395.2%

Reaction Steps

To a solution of 5-nitro-2-(4-(trifluoromethyl)phenyl)pyridine (260 mg, 0.97 mmol) in ethanol (10 mL) and tetrahydrofuran (5 mL) was added 10 wt % palladium on carbon (100 mg). The reaction was pressurized to 50 psi hydrogen and stirred at room temperature for 4 hours. The reaction was filtered through Celite and concentrated to give 6-(4-(trifluoromethyl)phenyl)pyridin-3-amine (220 mg, 95%). 1H NMR (400 MHz, CD3OD, δ): 7.98 (s, 1H), 7.88 (d, 2H), 7.60 (d2, H), 7.54 (d, 1H), 7.09 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056834B2
Source datasetuspto-grants-2015_06
ORD IDord-4fe3e4b817b04fb0b35903aaf0648dea
Source noteuspto-grants-2015_06