Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500498Generated: November 2, 2026

2-Bromobenzonitrile → 2-[3-(Aminomethyl)phenyl]benzonitrile hydrochloride

https://huagongshe.com/reaction/1500498

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromobenzonitrileHCID 16272—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantBoronic acid, B-(3-(aminomethyl)phenyl)-, hydrochloride (1:1)HCID 16427085—
SolventWater 1,2-dimethoxyethaneHCID 18180031—
Product2-[3-(Aminomethyl)phenyl]benzonitrile hydrochlorideHCID 11777812932.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 2-bromobenzonitrile (1.10 g), 3-aminomethylphenylboronic acid hydrochloride (1.13 g), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium-dichloromethane complex (0.10 g), and tripotassium phosphate (5.20 g) in a 4:1 dimethoxyethane-water mixed solvent (60 mL) was stirred at 70° C. for 3 hours. 2-Bromobenzonitrile (0.070 g) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium-dichloromethane complex (0.10 g) were added thereto, and the mixture was stirred at 70° C. for 2 hours. The reaction solution was cooled to room temperature, filtered through celite, and then separated into organic and aqueous layers. The organic layer was washed with a saturated aqueous sodium hydrogencarbonate solution and saturated saline, dried over anhydrous sodium sulfate, and then filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by chromatography on a silica gel column (Biotage Ltd., elution solvent: dichloromethane/methanol), and a fraction containing the desired compound was concentrated under reduced pressure. The obtained residue was dissolved in ethyl acetate, and concentrated hydrochloric acid was added to the solution. The resulting suspension was filtered, and the product collected by filtration was washed with ethyl acetate and dried under reduced pressure to obtain the title compound (0.483 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206168B2
Source datasetuspto-grants-2015_12
ORD IDord-0cf49d67f43f450bb038c993d326a66a
Source noteuspto-grants-2015_12