Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392059Generated: October 26, 2026

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

https://huagongshe.com/reaction/1392059

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 numberUS07342013B2
Source datasetuspto-grants-2008_03
ORD IDord-247c7f12546a44e5840e7efefe446a73
Source noteuspto-grants-2008_03