Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842851Generated: October 26, 2026

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

https://huagongshe.com/reaction/842851

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 SnCl2H2O (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 numberUS06376515B2
Source datasetuspto-grants-2002_04
ORD IDord-f7d8146bb7124ee79b84faef4ab93b6f
Source noteuspto-grants-2002_04