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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858020Generated: November 1, 2026

4-Nitro-3-phenethylaminobenzonitrile → 4-Amino-3-phenethylaminobenzonitrile

https://huagongshe.com/reaction/1858020

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitro-3-phenethylaminobenzonitrileHCID 22125499—
CatalystPalladiumHCID 23938—
SolventMeOH tetrahydrofuranHCID 21899815—
Product4-Amino-3-phenethylaminobenzonitrileHCID 22125554100%

Reaction Steps

A mixture comprising 3-methoxy-4-nitrobenzonitrile (1 g, 5.6 mmol), phenethylamine hydrochloride (1.8 g, 11.2 mmol), 50% sodium hydroxide (0.9 g, 11.2 mmol) and DMSO (3 mL) was heated at 100° C. for 3.5 hours, cooled and poured into a solution of 1N hydrochloric acid (200 mL, 0° C.). The mixture was stirred for 20 minutes to give a precipitate. The precipitate was collected and recrystallized from hot ethanol to provide 4-nitro-3-phenethylaminobenzonitrile (0.78 g, 2.9 mmol) as orange crystals. MS (CI), Calculated for C15H13N3O2, 267.3, Found (MH+): 282. A mixture comprising 4-nitro-3-phenethylaminobenzonitrile (0.75 g, 2.8 mmol), palladium on carbon (100 mg) and 1:1 methanol/THF (100 mL) was hydrogenated under 1 atm for 3 hours, filtered and concentrated under reduced pressure to provide 4-amino-3-phenethylaminobenzonitrile (0.68 g, 2.8 mmol) as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150379
Source datasetuspto-grants-2000_11
ORD IDord-30d747610aec4362b4fc0082bda1358a
Source noteuspto-grants-2000_11