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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842806Generated: November 2, 2026

4-(Bromomethyl)benzonitrile → HCID 14774146, compound

https://huagongshe.com/reaction/842806

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Bromomethyl)benzonitrileHCID 86996—
ReactantDiethylether waterHCID 21584184—
ReactantHCID 23684420HCID 23684420—
SolventDimethylformamideHCID 6228—
ProductHCID 14774146HCID 14774146—

Reaction Steps

A solution of 7.24 g (19.92 mmol) of sodium 3-(2quinolinylmethyloxy)phenoxide pentahydrate and 4.68 g (23.90 mmol) of p-cyanobenzyl bromide in 34 ml of dry DMF is stirred at 75° C. under nitrogen for 2 days. The reaction mixture is cooled to room temperature, then poured into 400 ml of 3:1 H2O/Et2O, shaken; and the phases separated. The aqueous layer is extracted and washed with 1:1 brine/H2O and brine. The ether solution is dried over 1:1 Na2SO4MgSO4, filtered and concentrated. The crude product is recrystallized from 70% EtOAc/hexane to obtain 4-(3-(2quinolinylmethyloxy)phenoxy-methyl)benzonitrile. (M.P. 112.5° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376512B1
Source datasetuspto-grants-2002_04
ORD IDord-a19f8d62b6be4581b2108e45c2c04c07
Source noteuspto-grants-2002_04