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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43327Generated: October 29, 2026

Sodium Carbonate → 5-(4-Chlorophenyl)-2-ethylaniline

https://huagongshe.com/reaction/43327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Chlorophenylboronic acidHCID 74299—
Reactant5-Bromo-2-ethylanilineHCID 23346756—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product5-(4-Chlorophenyl)-2-ethylanilineHCID 5944594588.2%

Reaction Conditions

Temperature20 °C

Reaction Steps

4-Chlorophenylboronic acid (13.2 g, 0.08 mol) and tetrakis(triphenylphosphine) palladium (0) (2.4 g, 0.002 mol) are added to a solution of 5-bromo-2-ethylaniline (14.1 g, 0.07 mol) in 1,2-dimethoxyethane (140 ml). After stirring the reaction mixture for 15 minutes at 20° C., a solution of 20% aqueous sodium carbonate (300 ml) is added to the mixture, and the resulting mixture is refluxed for 24 hours. The reaction mixture is cooled to room temperature, diluted with water and extracted using ethyl acetate. The combined organic extracts are dried over anhydrous sodium sulfate, filtered and the filtrate evaporated in vacuo. The residue is further purified by column chromatography on silica gel, eluting with 5% ethyl acetate in hexane to give 5-(4-chlorophenyl)-2-ethylaniline (14.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536351B2
Source datasetuspto-grants-2013_09
ORD IDord-9dc7fad2288147edbc64788618dc9274
Source noteuspto-grants-2013_09