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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131322Generated: October 25, 2026

2-Bromo-4-isopropylaniline → 2-Amino-5-isopropylbenzonitrile

https://huagongshe.com/reaction/131322

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4-isopropylanilineHCID 521337—
ReactantHCID 178418546HCID 178418546—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-Amino-5-isopropylbenzonitrileHCID 2109346388.5%

Reaction Steps

Heat a mixture of copper (I) cyanide (2.5 g, 28.02 mmol), and 2-bromo-4-isopropyl-phenylamine (5.0 g, 23.35 mmol) in 1-methyl-2-pyrrolidinone (20 ml) to 195° C. for four hours. Dilute the reaction mixture with 100 ml of ethyl acetate and the dark solution, wash twice with 28% aqueous ammonium hydroxide, twice with saturated aqueous sodium chloride (brine) and twice with water. Collect the organic layer, dry over sodium sulfate and remove the solvent under reduced pressure. Purify the via flash chromatography eluting with a step gradient starting with hexanes and going to 80% hexanes with 20% ethyl acetate to obtain 3.31 g (20.66 mmol, 88% yield) of the title compound as an orange oil: Mass Spectrum (m/e): 161(M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384934B2
Source datasetuspto-grants-2008_06
ORD IDord-ddbd8bc91ad648baaf64d5f6433256b3
Source noteuspto-grants-2008_06