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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181530Generated: October 26, 2026

3-(2-Nitrophenoxy)benzonitrile → 3-(2-Aminophenoxy)benzonitrile

https://huagongshe.com/reaction/1181530

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-Nitrophenoxy)benzonitrileHCID 9194888—
SolventEthanolHCID 702—
Product3-(2-Aminophenoxy)benzonitrileHCID 2259633599%

Reaction Steps

A solution of 3-(2-nitrophenoxy)benzonitrile (1.21 g, 5 mmol, 1.0 equiv) in 30 mL of EtOH was treated with SnCl22H2O (3.38 g, 3 equiv) at reflux for 4 h. The volatile was evaporated and the residue was redissolved in EtOAc, washed with saturated aqueous NaHCO3 and 1N NaOH. The organic layer was dried over MgSO4, filtered and evaporated to give 3-(2-aminophenoxy)benzonitrile (1.04 g, 99%). MS found for C13H11N2O (M+H)+: 211.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285565B2
Source datasetuspto-grants-2007_10
ORD IDord-88917d82f49e48f7913ecea2da4bc643
Source noteuspto-grants-2007_10