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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365713Generated: October 28, 2026

Methylamine → 2-(Methylamino)benzonitrile

https://huagongshe.com/reaction/365713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant2-FluorobenzonitrileHCID 67855—
SolventAcetonitrileHCID 6342—
Product2-(Methylamino)benzonitrileHCID 29260349%

Reaction Conditions

Temperature60 °C

Reaction Steps

2-Fluorobenzonitrile (10.0 g, 82.8 mmol) was dissolved in acetonitrile (100 ml), and 40% aqueous methylamine solution (200 ml) was added thereto, followed by stirring at 60° C. overnight. 40% aqueous methylamine solution (100 ml) was further added thereto, followed by stirring at 60° C. for 9 hours. The reaction mixture was concentrated under reduced pressure, then water was added to the resulting residue, the mixture was extracted with chloroform. After the organic layer was dried (over anhydrous magnesium sulfate), the drying agent was filtered off, and the organic layer was concentrated under reduced pressure. The resulting oily substances were purified by silica gel column chromatography (the substances were eluted with an increasing concentration of chloroform from chloroform/hexane=1/2 to chloroform/hexane=1/1) to give the title compound (5.38 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127541
Source datasetuspto-grants-2000_10
ORD IDord-ed01f4f1f1a24a719e725f3e2837e993
Source noteuspto-grants-2000_10