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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995821Generated: October 25, 2026

5-[(4-Chlorophenyl)methoxy]-2-nitropyridine → 5-[(4-Chlorophenyl)methoxy]pyridin-2-amine

https://huagongshe.com/reaction/1995821

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-[(4-Chlorophenyl)methoxy]-2-nitropyridineHCID 20486129—
CatalystWaterHCID 962—
SolventMethanolHCID 887—
Product5-[(4-Chlorophenyl)methoxy]pyridin-2-amineHCID 20486112—

Reaction Steps

A mixture of 5-(4-chlorobenzyloxy)-2-nitropyridine (0.5 g), Na2S (0.25 g) and methanol (12 ml) is heated to reflux for about 3 hours. Then, a few drops of water is added and refluxing continued about 15 hours. After cooling, the reaction is diluted with methanol, filtered through celite and stripped. The concentrate is taken up in CHCl3, washed with water, dried and stripped giving 2-amino-5-(4-chlorobenzyloxy)pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04406690
Source datasetuspto-grants-1983_09
ORD IDord-a45c41810db74af795ff44402984949c
Source noteuspto-grants-1983_09