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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710932Generated: October 26, 2026

3-Methoxy-2-nitropyridine → 2-Amino-3-methoxypyridine

https://huagongshe.com/reaction/710932

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methoxy-2-nitropyridineHCID 556063—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-Amino-3-methoxypyridineHCID 992038491%

Reaction Steps

A suspension of 3-methoxy-2-nitropyridin (30 g, 194.8 mmol) and 10% Pd/C (10 g) in ethanol (1 L) was hydrogenated in a par hydrogenator (H2, 40 psi pressure) at RT for 4 hours. The reaction mixture was filtered through celite and the filtrate was concentrated to afford the title compound (22 g, 91%, brown solid). 1H NMR (400 MHz, CDCl3): δ=7.66 (d, J=5.2 Hz; 1H), 6.91 (d, J=7.6 Hz, 1H), 6.63-6.60 (m, 1H), 4.65 (br, 2H), 3.84 (s, 3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181248B2
Source datasetuspto-grants-2015_11
ORD IDord-e32e3ca326f644b1bcccd6f89c60498d
Source noteuspto-grants-2015_11