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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341679Generated: October 25, 2026

4-Bromo-2-methylaniline → 4'-Chloro-3-methylbiphen-4-ylamine

https://huagongshe.com/reaction/341679

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-methylanilineHCID 11423—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chlorophenylboronic acidHCID 74299—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product4'-Chloro-3-methylbiphen-4-ylamineHCID 2300518870.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred, degassed solution of 4-bromo-2-methylaniline (20 g, 0.107 mol) in toluene (1200 ml) and ethanol (400 ml), under an atmosphere of nitrogen, is added 4-chlorophenylboronic acid (20.32 g, 0.13 mol) and the reaction mixture is stirred and heated to 80° C. Tetrakis(triphenylphosphine)palladium(0) (2.48 g, 0.002 mol) is added to the reaction mixture, and to this is added 2M aqueous potassium carbonate solution (160 ml). The reaction mixture is refluxed for 4 hours, then cooled to room temperature. The reaction mixture is filtered through diatomaceous earth, and the filtrate is evaporated under reduced pressure. The residue is partitioned between ethyl acetate and water. The aqueous phase is extracted with ethyl acetate (3×500 ml) and the organic extracts are combined and concentrated under reduced pressure to give 4′-chloro-3-methylbiphen-4-ylamine (16.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895761B2
Source datasetuspto-grants-2014_11
ORD IDord-9448fec464d840f59506ae2b53885044
Source noteuspto-grants-2014_11