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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027321Generated: October 30, 2026

Dimethylformamide → 1-(4-Methylphenyl)pyrene

https://huagongshe.com/reaction/1027321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTolylboronic acidHCID 79799—
Reactant1-BromopyreneHCID 159627—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Product1-(4-Methylphenyl)pyreneHCID 5783641185.7%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixed solution of 45.0 g of 1-bromopyrene, 21.7 g of 4-methylphenylboronic acid, 34.0 g of tripotassium phosphate, 10.3 g of tetrabutylammonium bromide, 0.71 g of palladium acetate and 1.6 L of dimethylformamide was heated with stirring under a nitrogen gas flow at 120° C. for 5 hours. After cooling to room temperature, 1.6 L of water was injected, followed by stirring at room temperature for 0.5 hours. The precipitated solid was collected by filtration and then washed twice with 200 ml of water. The resultant solid was dissolved in 500 ml of dichloromethane, dried over magnesium sulfate, evaporated and then filtered using Celite. The filtrate was evaporated and the residue was washed twice with 200 ml of methanol. The precipitated solid was collected by filtration and then vacuum-dried to obtain 40.0 g of 1-(4-methylphenyl)pyrene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729530B2
Source datasetuspto-grants-2014_05
ORD IDord-6bbe71f8d6044014b8ed61b3f0e18ccc
Source noteuspto-grants-2014_05