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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618826Generated: November 2, 2026

4,4'-Dibromobiphenyl → HCID 20650340, compound

https://huagongshe.com/reaction/1618826

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4'-DibromobiphenylHCID 7110—
ReactantBenzenamine, 4-methyl-N-(4-methylphenyl)-HCID 69293—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
ProductHCID 20650340HCID 206503403%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of tris(dibenzylideneacetone)dipalladium (353 mg, 0.385 mmol), and tri-tert-butyl phosphine (3.11 g of a 10% solution in hexanes) was degassed in toluene (anhydrous, 50 mL) for 20 minutes. Di-p-tolylamine (3.00 g, 15.2 mmol), and 4,4′-dibromobiphenyl (4.80 g, 15.4 mmol) were added and the mixture was further degassed for 15 minutes. Sodium tert-butoxide (2.4 g, 25 mmol) was added, and mixture was further degassed for 10 minutes. The whole was heated overnight at 120° C. under argon. After cooling, the mixture was poured into DCM, and solids were filtered off. Filtrate was washed with water and brine. The organic layer was collected and dried over sodium sulfate, then loaded onto silica gel. A flash column (gradient of 2-20% ethyl acetate in hexanes) gave 190 mg of material (3% yield); confirmed pure by HNMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08771845B2
Source datasetuspto-grants-2014_07
ORD IDord-980120f058804222bc174cd9a309d273
Source noteuspto-grants-2014_07