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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059967Generated: November 1, 2026

Ammonium Chloride → 2-Chloro-5-(4-methoxypyridin-2-yl)aniline

https://huagongshe.com/reaction/1059967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Chloro-4-(4-methoxypyridin-2-yl)-2-nitrobenzeneHCID 18667563—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-Chloro-5-(4-methoxypyridin-2-yl)anilineHCID 1866753298.1%

Reaction Steps

To a suspension of 1-chloro-4-(4-methoxypyridin-2-yl)-2-nitrobenzene (200 mg) in ethanol (6 ml) and water (0.6 ml) were added iron powder (206 mg) and ammonium chloride (28 mg), and the mixture was refluxed for 3 hours. The mixture was filtered, and the filtrate was evaporated under reduced pressure. To the residue were added ethyl acetate and water. The separated organic layer was washed with brine, dried over magnesium sulfate and evaporated under reduced pressure to give 2-chloro-5-(4-methoxypyridin-2-yl)aniline (174 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521643B1
Source datasetuspto-grants-2003_02
ORD IDord-4504a36a778c4eb1963c155955dad364
Source noteuspto-grants-2003_02