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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926418Generated: October 26, 2026

Silane, (4-bromophenyl)trimethyl- → 4-phenyl-2,5-difluoro-N-(4-trimethylsilylphenyl)benzenamine

https://huagongshe.com/reaction/926418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSilane, (4-bromophenyl)trimethyl-HCID 138897—
ReactantSodiumHCID 5360545—
Reactant4-Phenyl-2,5-difluoroanilineHCID 46314621—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product4-phenyl-2,5-difluoro-N-(4-trimethylsilylphenyl)benzenamineHCID 5809923173.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-phenyl-2,5-difluoroaniline (12 mmol), 4-bromo-trimethylsilylbenzene (10 mmol), tris(dibenzylideneacetone)dipalladium(0) (0.15 mmol), (±)-2,2′-bis(diphenylphosphine)-1,1′-binaphthalene (0.3 mmol) and sodium tert-butoxie (14 mmol) are put in a two-neck round-bottom flask and dissolved in toluene (30 mL). Subsequently, the resulting solution is stirred in a bath under a temperature of about 100° C. for 24 hours. After completion of the reaction, toluene is removed. The reaction mixture is extracted with dichloromethane and water, and then being distilled under reduced pressure. The resulting residence is filtered by silica gel column and distilled under reduced pressure again. Next, by re-crystallizing and filtering with dichloromethane and petroleum ether, 4-phenyl-2,5-difluoro-N-(4-trimethylsilylphenyl)benzenamine (2.6 g) is yielded.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284486B2
Source datasetuspto-grants-2016_03
ORD IDord-3d2a849917d6437193f10944d561968b
Source noteuspto-grants-2016_03