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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027313Generated: October 29, 2026

Dimethylformamide → 1-(2-Naphthyl)pyrene

https://huagongshe.com/reaction/1027313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-BromopyreneHCID 159627—
Reactant(Naphthalen-2-yl)boronic acidHCID 2734375—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Product1-(2-Naphthyl)pyreneHCID 5404735091.7%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixed solution of 7.0 g of 1-bromopyrene, 4.7 g of 2-naphthaleneboronic acid, 11.6 g of tripotassium phosphate, 1.8 g of tetrabutylammonium bromide, 0.11 g of palladium acetate and 248 ml of dimethylformamide was heated with stirring under a nitrogen gas flow at 130° C. for 5 hours. After cooling the solution to room temperature, 300 ml 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 100 ml of water. The resultant solid was dissolved in 200 ml of dichloromethane, dried over magnesium sulfate, evaporated and then filtered using Celite. The filtrate was evaporated and the residue was washed twice with 100 ml of methanol, and then the precipitated solid was collected by filtration. The solid was vacuum-dried to obtain 7.5 g of 1-(2-naphthyl)pyrene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729530B2
Source datasetuspto-grants-2014_05
ORD IDord-74b2e57a6edd4d2396943891541c0bc1
Source noteuspto-grants-2014_05