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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365715Generated: October 31, 2026

Benzylamine → 4-(Benzylamino)benzonitrile

https://huagongshe.com/reaction/365715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant4-FluorobenzonitrileHCID 14517—
SolventAcetonitrileHCID 6342—
Product4-(Benzylamino)benzonitrileHCID 994250972%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-Fluorobenzonitrile (6.0 g, 49.5 mmol) was dissolved in acetonitrile (60 ml), and benzylamine (10.6 g, 98.9 mmol) was added thereto, followed by stirring at 100° C. for 3 days. To complete the reaction, benzylamine (21.2 g, 198 mmol) was further added thereto, followed by stirring at 100° C. for 1 day. The solvent was removed under reduced pressure, water was added to the resulting residue, and the mixture was extracted with chloroform. After the organic layer was dried (over anhydrous magnesium sulfate), the drying agent was filtered off, and the filtrate 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 (7.42 g, 72%) as oily substances.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127541
Source datasetuspto-grants-2000_10
ORD IDord-c62496db747b455c93fae36e6f33e695
Source noteuspto-grants-2000_10