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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1412588Generated: October 25, 2026

Dichloromethane → 4'-Formyl-2'-nitrobiphenyl-2-carbonitrile

https://huagongshe.com/reaction/1412588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
Reactant4-Bromo-3-nitrobenzaldehydeHCID 808792—
Reactant2-Cyano-phenylboric acidHCID 21708089—
CatalystTetrabutylammonium BromideHCID 74236—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventTolueneHCID 1140—
Product4'-Formyl-2'-nitrobiphenyl-2-carbonitrileHCID 8664407447%

Reaction Steps

A mixture of 4-bromo-3-nitrobenzaldehyde (10.0 g), 2-cyanophenylboric acid (8.25 g), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II), dichloromethane adduct (3.45 g), tetrabutylammonium bromide (1.36 g), 2M aqueous sodium carbonate solution (40 mL) and toluene (400 mL) was refluxed under an argon atmosphere for 3 days. The reaction mixture was concentrated, and the residue was dissolved in ethyl acetate. The obtained ethyl acetate solution was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the title compound as a pale-yellow solid (5.15 g, 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921379B2
Source datasetuspto-grants-2014_12
ORD IDord-df8ab092ab654372838335df57731c8e
Source noteuspto-grants-2014_12