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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914400Generated: November 2, 2026

Dimethylformamide → 1-(3,5-Dichlorophenyl)-6-(4-methylphenyl)pyrene

https://huagongshe.com/reaction/1914400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant3,5-Dichlorophenylboronic acidHCID 2734331—
Reactant1-Bromo-6-(4-methylphenyl)pyreneHCID 86101361—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Product1-(3,5-Dichlorophenyl)-6-(4-methylphenyl)pyreneHCID 8610138158.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixed solution of 8.0 g of 1-bromo-6-(4-methylphenyl)pyrene, 4.5 g of 3,5-dichlorophenylboronic acid, 9.2 g of tripotassium phosphate, 1.4 g of tetrabutylammonium bromide, 97 mg of palladium acetate and 215 ml of dimethylformamide was heated and stirred under a nitrogen gas stream at 120° C. for 5 hours. The solution was cooled to room temperature and 1.0 L of water was poured into the solution, followed by extraction with 600 ml of dichloromethane. The organic layer was washed twice with 200 ml of water, dried over magnesium sulfate and then filtered through Celite. The filtrate was evaporated and the residue was washed twice with 200 ml of ethyl acetate, and then the precipitated solid was collected by filtration. The precipitated solid was recrystallized from 100 ml of dimethylformamide and then vacuum-dried to obtain 5.5 g of 1-(3,5-dichlorophenyl)-6-(4-methylphenyl)pyrene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08610345B2
Source datasetuspto-grants-2013_12
ORD IDord-52661c09f5294f2fb52ef56def469bcd
Source noteuspto-grants-2013_12