Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400372Generated: October 29, 2026

Sodium Carbonate → 4'-Chloro-4-ethyl-3-nitrobiphenyl

https://huagongshe.com/reaction/400372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Chlorophenylboronic acidHCID 74299—
Reactant4-Bromo-1-ethyl-2-nitrobenzeneHCID 7566996—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4'-Chloro-4-ethyl-3-nitrobiphenylHCID 59445932104.7%

Reaction Conditions

Temperature20 °C

Reaction Steps

To 4-bromo-1-ethyl-2-nitrobenzene (20.0 g, 0.087 mol) in 150 ml 1,2-dimethoxyethane is added, at room temperature, 4-chlorophenylboronic acid (14.98 g, 0.096 mol) and tetrakis(triphenylphosphine)palladium(0) (2.0 g, 0.00174 mol) and nitrogen gas is bubbled through the mixture. After stirring for 10 minutes at 20° C., a solution of sodium carbonate (73.8 g, 0.696 mol) in water (350 ml) is added and mixture is refluxed for 16 hours. The reaction mixture is cooled to room temperature, filtered through diatomaceous earth, washing with 200 ml of ethyl acetate. The mixture is poured into a separating funnel and the two phases are separated. The aqueous phase is extracted with ethyl acetate. The organic extracts are combined, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated in vacuo to give 4′-chloro-4-ethyl-3-nitrobiphenyl (23.84 g) as a brown oil used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741806B2
Source datasetuspto-grants-2014_06
ORD IDord-72c1feda0ee1403b9f48c253ac7bd01f
Source noteuspto-grants-2014_06