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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209462Generated: October 26, 2026

Water → 2-bromo-4-(4-pyridinylmethyl)Benzenamine

https://huagongshe.com/reaction/2209462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant4-[(Pyridin-4-yl)methyl]anilineHCID 307158—
SolventDimethylformamideHCID 6228—
SolventAluminumHCID 5359268—
Product2-bromo-4-(4-pyridinylmethyl)BenzenamineHCID 2186564577.3%

Reaction Steps

A solution of N-bromosuccinimide (1.4 gm) in 10 mL dimethylformamide was added in a dropwise manner to a solution of 4-(4-aminobenzyl)pyridine (1.5 gm) in 10 mL of dimethylformamide. The reaction flask was wrapped in aluminum foil to prevent exposure of the reagents to light. The reaction mixture was stirred at room temperature for 3 hours. The progress of the reaction was monitored by thin-layer chromatography. When the reaction was completed, the reaction mixture was combined with 100 mL of H2O with stirring. A reddish brown precipitate was formed, filtered out of solution, washed with H2O, and air dried. The solid was dissolved in ethyl acetate, back washed with saturated NaCl, dried over MgSO4 and triturated with ethyl ether. The solid was filtered from the solution and air dried yielding 1.6 gm of 4-(4-amino-3-bromobenzyl)pyridine as reddish/tan crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455252
Source datasetuspto-grants-1995_10
ORD IDord-29c5a1d3b02141a78591019cf7cdb68e
Source noteuspto-grants-1995_10