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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440382Generated: October 26, 2026

2-Bromobenzonitrile → 2-(5-Methylbenzofuran-2-yl)benzonitrile

https://huagongshe.com/reaction/1440382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromobenzonitrileHCID 16272—
Reactant1,1-Dimethylethyl [2-[3-bromo-5-(bromomethyl)-2-benzofuranyl]phenyl]carbamateHCID 11754925—
SolventDiethyl EtherHCID 3283—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium BicarbonateHCID 516892—
Product2-(5-Methylbenzofuran-2-yl)benzonitrileHCID 15680844109.1%

Reaction Steps

Intermediate 1 (20 g) was added to a stirred solution of 2-bromobenzonitrile (10.34 g) and tetrakistriphenylphosphine palladium (0) (1.5 g) in DME (200 ml) and 8% aqueous NaHCO3 (50 ml) at reflux under nitrogen. Further catalyst (1.5 g) was added and the reaction was heated overnight. The reaction was cooled to room temperature and diluted with ether (200 ml). The organic layer was separated, washed with water (3×100 ml) and dried. Filtration and evaporation gave a white solid which was purified by chromatography eluting with System A (1:9) to give the title compound (10.58 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498722
Source datasetuspto-grants-1996_03
ORD IDord-9682abf11de5410d956a16e18da3f0d7
Source noteuspto-grants-1996_03