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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515228Generated: November 2, 2026

Ammonium Chloride → 4-(Pyridin-3-Yloxy)Aniline

https://huagongshe.com/reaction/1515228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant3-(4-Nitrophenoxy)pyridineHCID 119902—
CatalystIronHCID 23925—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-(Pyridin-3-Yloxy)AnilineHCID 315963136%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-(Pyridin-3-yl)oxy-1-nitrobenzene prepared in Step A was dissolved in the mixture of water (100 mL), tetrahydrofuran (100 mL) and methanol (100 mL). Iron powder (103 g, 1.84 mol) and ammonium chloride (99 g, 1.84 mol) were added thereto, and the mixture was stirred for 3 h at 80° C. using a mechanical stirrer. After completion of the reaction, the reaction mixture was filtered through a cellite, washed with methanol, and concentrated under reduced pressure. The solid thus obtained was filtered, washed with ether, and dried to give the title compound (17 g, Yield 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222414B2
Source datasetuspto-grants-2012_07
ORD IDord-67ee1148b03b406f96dcbf466b0cc7c1
Source noteuspto-grants-2012_07