Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864330Generated: October 31, 2026

2-Methyl-5-(2-methyl-4-nitrophenoxy)pyridine → 3-Methyl-4-((6-methylpyridin-3-yl)oxy)aniline

https://huagongshe.com/reaction/1864330

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-5-(2-methyl-4-nitrophenoxy)pyridineHCID 17990102—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product3-Methyl-4-((6-methylpyridin-3-yl)oxy)anilineHCID 1142443498%

Reaction Steps

A mixture of 2-methyl-5-(2-methyl-4-nitrophenoxy)pyridine (141 g, 0.58 mol) and 10% palladium on charcoal (13 g) in ethyl acetate (200 ml) and ethanol (700 ml) was stirred under an atmosphere of hydrogen (1.2 bar) for 5 hours. After reaction completion, the mixture was purged with nitrogen and the catalyst was filtered off. The filtrate was evaporated to dryness to give 3-methyl-4-[(6-methylpyridin-3-yl)oxy]aniline (120.6 g, 98%) as a white solid; Mass spectrum MH+ 215.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625908B2
Source datasetuspto-grants-2009_12
ORD IDord-50d22c48aa9846feacf39883ddce3406
Source noteuspto-grants-2009_12