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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609855Generated: October 26, 2026

Aniline → 2-Aminophenyl-4-nitro-benzonitrile

https://huagongshe.com/reaction/1609855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloro-4-nitrobenzonitrileHCID 141401—
SolventEthyl AcetateHCID 8857—
Product2-Aminophenyl-4-nitro-benzonitrileHCID 1794795788.4%

Reaction Steps

2-Chloro-4-nitro-benzonitrile (Aldrich) (3.64 g, 20 mmol), aniline (2 mL, 22 mmol), 1-methyl-2-pyrollidinone (10 mL) and diisopropylethylamine (4 mL) were combined and heated to 120° under Ar for 18 h, cooler poured into EtOAc (150 mL), washed with H20 (3×50 mL) and satd aq NaCl (50 mL), dried (Na2SO4), concentrated, and the residue was triturated with hexane, filtered and the solid was washed with hexane and dried in vacuo to afford 4.23 g (88%) of the title compound as a light green solid. 1H NMR (400) MHz, δ: 8.45 (finely split doublet, 1), 8.19 (dd, 1), 7.48 (m,3), 7.28 (d,2), 7.06 (d,1), 6.96 (br s,1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982270B1
Source datasetuspto-grants-2006_01
ORD IDord-5a79adfa8994446aaeb07317d99fe9e9
Source noteuspto-grants-2006_01