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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249493Generated: October 30, 2026

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

https://huagongshe.com/reaction/2249493

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 C13H, N2O (M+H)+: 211.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314874B2
Source datasetuspto-grants-2008_01
ORD IDord-5aba778e749c4be38625610a6abf5eab
Source noteuspto-grants-2008_01